{"id":7524,"date":"2026-05-08T08:27:00","date_gmt":"2026-05-08T00:27:00","guid":{"rendered":"https:\/\/runjiapaper.com\/?p=7524"},"modified":"2026-05-06T16:31:17","modified_gmt":"2026-05-06T08:31:17","slug":"fda-compliant-manufacturer-audit-checklist-2026-us","status":"publish","type":"post","link":"https:\/\/runjiapaper.com\/zh\/fda-compliant-manufacturer-audit-checklist-2026-us\/","title":{"rendered":"FDA-Compliant Manufacturer Audit Checklist for 2026 US Importers"},"content":{"rendered":"<p><script type=\"application\/ld+json\">{\n    \"@context\": \"https:\\\/\\\/schema.org\",\n    \"@graph\": [\n        {\n            \"@type\": \"Article\",\n            \"headline\": \"FDA-Compliant Manufacturer Audit Checklist for 2026 US Importers\",\n            \"author\": {\n                \"@type\": \"Person\",\n                \"name\": \"Tracy\",\n                \"url\": \"https:\\\/\\\/runjiapaper.com\\\/about\\\/\"\n            },\n            \"datePublished\": \"2026-04-28\",\n            \"dateModified\": \"2026-04-28\",\n            \"publisher\": {\n                \"@type\": \"Organization\",\n                \"name\": \"Runjia New Material\",\n                \"url\": \"https:\\\/\\\/runjiapaper.com\"\n            }\n        },\n        {\n            \"@type\": \"Organization\",\n            \"name\": \"Runjia New Material\",\n            \"url\": \"https:\\\/\\\/runjiapaper.com\",\n            \"sameAs\": [\n                \"https:\\\/\\\/www.linkedin.com\\\/company\\\/runjia-new-material\\\/\"\n            ]\n        },\n        {\n            \"@type\": \"Person\",\n            \"name\": \"Tracy\",\n            \"jobTitle\": \"Export Manager\",\n            \"worksFor\": {\n                \"@type\": \"Organization\",\n                \"name\": \"Runjia New Material\"\n            },\n            \"knowsAbout\": [\n                \"FDA 21 CFR 176.170\",\n                \"food contact compliance audit\",\n                \"FCN notification\"\n            ]\n        }\n    ]\n}<\/script><\/p>\n<style>\nhtml{scroll-behavior:smooth}\n.bp-wrap{max-width:980px;margin:0 auto;font-family:\"Nunito\",\"Avenir Next\",\"Helvetica Neue\",Arial,sans-serif;line-height:1.8;color:#24303f}\n.bp-wrap h1,.bp-wrap h2,.bp-wrap h3{color:#1f2937;line-height:1.35;letter-spacing:.2px}\n.bp-wrap h1{font-size:36px;margin-bottom:18px;font-weight:800}\n.bp-wrap h2{font-size:29px;margin-top:42px;margin-bottom:16px;font-weight:800}\n.bp-wrap h3{font-size:22px;margin-top:28px;margin-bottom:12px;font-weight:700}\n.bp-wrap p{margin:0 0 16px;font-size:16px}\n.bp-wrap ul,.bp-wrap ol{margin:0 0 18px 24px}\n.bp-wrap li{margin-bottom:8px}\n.bp-wrap a{color:#b7791f;text-decoration:none;font-weight:700}\n.bp-wrap a:hover{text-decoration:underline}\n.bp-hero{background:linear-gradient(135deg,#f7f4ee 0%,#fffaf2 100%);border:1px solid #eadfce;border-radius:18px;padding:30px;margin-bottom:28px;box-shadow:0 8px 24px rgba(31,41,55,.05)}\n.bp-highlight{background:#fff8ec;border-left:5px solid #d59b2d;padding:18px 20px;margin:24px 0;border-radius:10px}\n.bp-checklist{background:#f9fafb;border:1px solid #e5e7eb;border-radius:16px;padding:22px;margin:22px 0}\n.bp-table-wrap{overflow-x:auto;margin:22px 0 28px}\n.bp-table{width:100%;border-collapse:collapse;font-size:15px;min-width:760px;background:#fff;border-radius:14px;overflow:hidden}\n.bp-table th,.bp-table td{border:1px solid #dbe3ea;padding:13px 14px;text-align:left;vertical-align:top}\n.bp-table th{background:#f3f4f6;font-weight:800}\n.bp-box{background:#f8fafc;border:1px solid #dbe3ea;border-radius:16px;padding:22px;margin:24px 0}\n.bp-faq{background:#fff;border:1px solid #e5e7eb;border-radius:16px;padding:24px;margin:18px 0;box-shadow:0 8px 24px rgba(31,41,55,.04)}\n.bp-cta{background:linear-gradient(135deg,#1f2937 0%,#334155 100%);color:#fff;border-radius:20px;padding:32px 28px;margin-top:42px;box-shadow:0 12px 32px rgba(31,41,55,.16)}\n.bp-cta h2,.bp-cta h3,.bp-cta p,.bp-cta li{color:#fff}\n.bp-cta a{color:#f7d08a}\n.bp-btn{display:inline-block;background:#d59b2d;color:#fff!important;text-decoration:none;padding:14px 24px;border-radius:999px;font-weight:800;margin-top:12px;box-shadow:0 8px 18px rgba(213,155,45,.28)}\n.bp-note{font-size:14px;color:#d1d5db}\n.bp-image{margin:24px 0 30px;text-align:center}\n.bp-image img{width:100%;max-width:100%;height:auto;border-radius:18px;display:block;box-shadow:0 12px 28px rgba(31,41,55,.08)}\n.bp-image-caption{font-size:14px;color:#6b7280;margin-top:10px}\n.bp-link-row{margin-top:18px;display:flex;flex-wrap:wrap;gap:10px 18px}\n.bp-source{font-size:15px;color:#4b5563;margin-top:10px}\n.bp-experience{background:#f0f7ff;border-left:4px solid #2196F3;padding:20px 24px;margin:32px 0;border-radius:4px}\n.bp-experience h3{margin-top:0;color:#1565C0}\n<\/style>\n<div class=\"bp-wrap\">\n<h1>FDA-Compliant Manufacturer Audit Checklist for 2026 US Importers<\/h1>\n<div class=\"bp-image\">\n<img decoding=\"async\" src=\"https:\/\/runjiapaper.com\/wp-content\/uploads\/2026\/05\/fda-compliant-manufacturer-9-document-presentation-v2-2026.jpg\" alt=\"FDA-compliant manufacturer 9-document audit pack presentation with US importer compliance team meeting\"><\/p>\n<div class=\"bp-image-caption\">9-document audit pack presentation with US importer compliance team &mdash; this is what a real FDA-compliant manufacturer ships unprompted with every container.<\/div>\n<\/div>\n<p><strong>The short answer: a US importer auditing an FDA-compliant manufacturer in 2026 must verify nine documents \u2014 21 CFR 176.170 compliance letter on factory letterhead, 175.300 silicone declaration, FCN list reference, GMP attestation under 21 CFR 174-178, recent SGS migration test, PFAS-free TOF report, FDA establishment registration number, supplier verification program documentation under FSMA, and a state-specific PFAS attestation for CA\/NY\/ME\/WA\/MN.<\/strong> An FDA-compliant manufacturer that cannot produce these nine documents in PDF within 24 hours of request is not actually FDA-compliant \u2014 it is a converter that hopes upstream suppliers are. This guide walks through each document, what to look for, and the specific phrases that indicate a fake FDA-compliant manufacturer claim.<\/p>\n<div class=\"bp-hero\">\n<h2 style=\"margin-top:0;\">Why a 9-document FDA-compliant manufacturer audit matters in 2026<\/h2>\n<p>FDA enforcement of food contact paper compliance has tightened materially since the <a href=\"https:\/\/www.fda.gov\/food\/process-contaminants-food\/authorized-uses-pfas-food-contact-applications\" target=\"_blank\" rel=\"noopener noreferrer\">February 2024 voluntary PFAS phase-out announcement<\/a>. Customs and Border Protection now flags shipments lacking complete documentation at random rates of 8&ndash;12% on HS 4811 entries from China \u2014 up from under 2% pre-2024. State-level PFAS bills (CA AB 1200, NY S.501-B, ME LD 1503) add a second documentation layer. A 2026 US importer that cannot produce the nine-document FDA-compliant manufacturer pack on customs inquiry pays detention costs of $200&ndash;$350 per day per container.<\/p>\n<\/div>\n<div class=\"bp-highlight\">\n<strong>Quick takeaway for compliance officers auditing an FDA-compliant manufacturer:<\/strong><\/p>\n<ul>\n<li><strong>9 must-have documents:<\/strong> See list below \u2014 every FDA-compliant manufacturer should ship them with each container<\/li>\n<li><strong>Letterhead test:<\/strong> All documents on the FDA-compliant manufacturer&rsquo;s own letterhead, never on third-party letterhead<\/li>\n<li><strong>Date freshness:<\/strong> Migration test &lt;12 months, PFAS test &lt;12 months, GMP attestation &lt;24 months<\/li>\n<li><strong>Cost of skipping audit:<\/strong> $200&ndash;$350\/day detention + $24K&ndash;$32K rejection cost vs $0 audit cost<\/li>\n<li><strong>Verification time:<\/strong> Full audit takes 30&ndash;45 minutes of email exchange<\/li>\n<\/ul>\n<\/div>\n<h2>The 9-document audit checklist for any FDA-compliant manufacturer<\/h2>\n<h3>Document 1: 21 CFR 176.170 compliance letter on factory letterhead<\/h3>\n<p>The cornerstone document. Cites the specific FDA regulation governing components of paper and paperboard intended for food contact. A real FDA-compliant manufacturer issues this on its own letterhead, naming the factory address and FDA establishment registration number. A trading company forwards a similar letter from upstream &mdash; instantly identifiable by the third-party letterhead.<\/p>\n<h3>Document 2: 21 CFR 175.300 declaration for silicone coating<\/h3>\n<p>Required for any silicone coated paper. Cites the FDA regulation governing resinous and polymeric coatings used in food contact. The silicone supplier brand (Dow, Wacker, Shin-Etsu, Elkem) should be named in the declaration. An FDA-compliant manufacturer that hides the silicone brand is hiding the chemistry &mdash; reject.<\/p>\n<h3>Document 3: FCN (Food Contact Notification) list reference<\/h3>\n<p>Some food contact materials are covered by FCNs (Food Contact Notifications) rather than the broader CFR. A serious FDA-compliant manufacturer references applicable FCN numbers if its silicone or coating chemistry is FCN-covered. <a href=\"https:\/\/www.fda.gov\/food\/inventory-effective-food-contact-substance-fcs-notifications\" target=\"_blank\" rel=\"noopener noreferrer\">The FDA FCN inventory is publicly searchable<\/a>.<\/p>\n<h3>Document 4: GMP attestation under 21 CFR Part 174-178<\/h3>\n<p>Good Manufacturing Practice attestation confirms the FDA-compliant manufacturer follows the food-grade production standards required under FDA. Should reference internal GMP procedures, sanitation schedule, allergen control program, and traceability system.<\/p>\n<h3>Document 5: Recent SGS or Intertek migration test report (&lt;12 months)<\/h3>\n<p>Required by EU 10\/2011 cross-referenced into FDA practice. Total migration &lt;10 mg\/dm&sup2; in fat simulant D2 (vegetable oil) and aqueous simulant A. The specific SKU being shipped must match the test &mdash; a sister-SKU test does not pass audit.<\/p>\n<h3>Document 6: PFAS-free TOF (Total Organic Fluorine) test report<\/h3>\n<p>Beyond federal voluntary phase-out, state PFAS bills require &lt;100 ppm TOF (some states require zero intentional). An FDA-compliant manufacturer ships the latest SGS or Intertek TOF report with each batch. See our companion guide on <a href=\"https:\/\/runjiapaper.com\/zh\/baking-paper\/\">PFAS-free baking paper manufacturer sourcing<\/a> for state-by-state thresholds.<\/p>\n<h3>Document 7: FDA establishment registration number<\/h3>\n<p>Foreign FDA-compliant manufacturers must register their facility with the FDA under FFDCA section 415. The registration number should be printed on the 176.170 compliance letter. <a href=\"https:\/\/www.fda.gov\/food\/registration-food-facilities-and-other-submissions\/fda-industry-systems\" target=\"_blank\" rel=\"noopener noreferrer\">Verify via FDA Industry Systems<\/a> &mdash; takes 60 seconds.<\/p>\n<h3>Document 8: FSMA Foreign Supplier Verification Program (FSVP) documentation<\/h3>\n<p>Under FSMA, US importers are required to verify foreign suppliers. A real supplier prepares the FSVP package: hazard analysis, supplier evaluation, risk-based supplier verification activities, written records. Pre-prepared FSVP package is a strong sign of The factory maturity.<\/p>\n<h3>Document 9: State-specific PFAS attestation (CA \/ NY \/ ME \/ WA \/ MN)<\/h3>\n<p>Five US states have their own PFAS attestation requirements separate from federal. A real manufacturer serving the US market issues a single combined attestation citing all five state bills explicitly. Generic &ldquo;PFAS-free&rdquo; claims do not satisfy state-level audit.<\/p>\n<div class=\"bp-image\">\n<img decoding=\"async\" src=\"https:\/\/runjiapaper.com\/wp-content\/uploads\/2026\/05\/fda-compliant-manufacturer-establishment-registration-v2-2026.jpg\" alt=\"FDA-compliant manufacturer establishment registration number verification on FDA Industry Systems with buyer team\"><\/p>\n<div class=\"bp-image-caption\">FDA establishment registration verification on FDA Industry Systems with US buyer team &mdash; 60-second test to confirm a real FDA-compliant manufacturer.<\/div>\n<\/div>\n<h2>The audit script: 5 emails to fully audit an A compliant supplier<\/h2>\n<ol>\n<li><strong>Email 1:<\/strong> Request all 9 documents in one combined PDF. Real The supplier responds within 24 hours.<\/li>\n<li><strong>Email 2:<\/strong> Verify FDA establishment registration number via FDA Industry Systems (free public lookup).<\/li>\n<li><strong>Email 3:<\/strong> Cross-check migration test report&rsquo;s SKU number against the SKU you are sourcing &mdash; reject if mismatched.<\/li>\n<li><strong>Email 4:<\/strong> Ask The factory to name the silicone brand and base paper mill in writing &mdash; should match Document 2 and Document 4.<\/li>\n<li><strong>Email 5:<\/strong> Request a video call with the This manufacturer&rsquo;s QC manager to walk through the QC procedure document referenced in Document 4.<\/li>\n<\/ol>\n<p>Total elapsed time: 3&ndash;5 working days. Cost: $0. Value: filters out 60&ndash;70% of self-described &ldquo;The manufacturer&rdquo; candidates that cannot actually back the claim.<\/p>\n<div class=\"bp-experience\">\n<h3>\ud83c\udfed From Our Factory Floor<\/h3>\n<p><strong>Real case (April 2026):<\/strong> A US importer at Canton Fair Phase 2 had been quoted by 6 suppliers for an air fryer liner private label program. They asked Runjia and the other 5 suppliers for the same 9-document A compliant supplier pack with a 24-hour deadline. Runjia delivered all 9 documents in a 14 MB combined PDF on the same day. Two other suppliers delivered partial packs in 48&ndash;72 hours. Three suppliers either did not respond or sent generic marketing PDFs. The buyer eliminated 4 suppliers and proceeded to sample with the 2 remaining The supplier candidates. Runjia won the order three weeks later.<\/p>\n<p><strong>What we learned:<\/strong> The 9-document audit is the single fastest filter for The factory claims. We ship the combined PDF unprompted with every initial sample request now. Sample-to-PI conversion rate climbed from 41% to 68% in the 12 months after we made this change. Compliance documentation is no longer a back-office function &mdash; it is a sales accelerator.<\/p>\n<\/div>\n<h2>Common This manufacturer red flags in 2026 audits<\/h2>\n<ul>\n<li><strong>&ldquo;FDA approved&rdquo; phrasing.<\/strong> The FDA does not approve papers \u2014 it sets compliance standards. The correct phrase is &ldquo;The manufacturer per 21 CFR 176.170&rdquo;<\/li>\n<li><strong>Generic &ldquo;food grade&rdquo; certificates without CFR citation<\/strong><\/li>\n<li><strong>Migration test reports older than 18 months<\/strong><\/li>\n<li><strong>Silicone declaration with no named silicone supplier<\/strong><\/li>\n<li><strong>FDA establishment registration number that does not appear in FDA Industry Systems lookup<\/strong><\/li>\n<li><strong>FSVP documentation that says &ldquo;not applicable&rdquo;<\/strong> &mdash; FSVP applies to all foreign A compliant supplier shipments<\/li>\n<li><strong>State PFAS attestation citing only one or two states<\/strong> &mdash; should cover all five state bills<\/li>\n<\/ul>\n<h2>Pricing: a real supplier charges 4&ndash;8% more, justified<\/h2>\n<p>The premium for a fully The factory (vs an opportunistic competitor that promises but cannot prove) runs 4&ndash;8% on FOB carton pricing. The premium covers ongoing testing fees, FDA registration maintenance, FSVP documentation labor, and GMP audit preparation. Recovered within 1&ndash;2 shipments through avoided detention and rejection costs.<\/p>\n<div class=\"bp-table-wrap\">\n<table class=\"bp-table\">\n<thead>\n<tr>\n<th>SKU (8K ctn)<\/th>\n<th>Non-compliant supplier FOB<\/th>\n<th>This manufacturer FOB<\/th>\n<th>Premium<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td><a href=\"https:\/\/runjiapaper.com\/zh\/air-fryer-parchment-paper-liner\/\">Air fryer liner 7.5&Prime;<\/a><\/td>\n<td>$7.10<\/td>\n<td>$7.50<\/td>\n<td>5.6%<\/td>\n<\/tr>\n<tr>\n<td>Baking sheet 12&Prime;&times;16&Prime;<\/td>\n<td>$9.80<\/td>\n<td>$10.40<\/td>\n<td>6.1%<\/td>\n<\/tr>\n<tr>\n<td><a href=\"https:\/\/runjiapaper.com\/zh\/parchment-paper\/\">Parchment roll 15m&times;30cm<\/a><\/td>\n<td>$13.20<\/td>\n<td>$14.10<\/td>\n<td>6.8%<\/td>\n<\/tr>\n<tr>\n<td>Jumbo roll 38gsm<\/td>\n<td>$45<\/td>\n<td>$48<\/td>\n<td>6.7%<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<div class=\"bp-box\">\n<h3 style=\"margin-top:0;\">Buyer questions a real manufacturer should answer in the first email<\/h3>\n<ul>\n<li>Send all 9 audit documents in one PDF within 24 hours<\/li>\n<li>Confirm your FDA establishment registration number for FDA Industry Systems verification<\/li>\n<li>Name the silicone supplier brand and the base paper mill<\/li>\n<li>Send your most recent SGS\/Intertek migration test on this exact SKU<\/li>\n<li>Send your state PFAS attestation covering CA, NY, ME, WA, MN<\/li>\n<\/ul>\n<\/div>\n<h2>FAQ for US compliance officers<\/h2>\n<div class=\"bp-faq\">\n<h3>What is the difference between &ldquo;FDA approved&rdquo; and &ldquo;A compliant supplier&rdquo;?<\/h3>\n<p>&ldquo;FDA approved&rdquo; is incorrect terminology &mdash; the FDA does not approve foodservice papers. &ldquo;The supplier&rdquo; is correct: the manufacturer&rsquo;s product meets the FDA regulation 21 CFR 176.170 (paper) and 175.300 (silicone coating). Suppliers using &ldquo;FDA approved&rdquo; phrasing are usually not actually compliant; they are using marketing copy.<\/p>\n<\/div>\n<div class=\"bp-faq\">\n<h3>Does a real factory need to register with the FDA?<\/h3>\n<p>Yes &mdash; under FFDCA section 415, every foreign facility that manufactures food contact materials for export to the US must register with the FDA. The registration number must appear on shipping documents. A self-described This manufacturer without a verifiable registration number is not actually FDA-compliant.<\/p>\n<\/div>\n<div class=\"bp-faq\">\n<h3>How does FSMA affect The manufacturer audits in 2026?<\/h3>\n<p>The Foreign Supplier Verification Program (FSVP) under FSMA requires US importers to verify their foreign suppliers actually meet FDA requirements. An experienced A compliant supplier prepares the FSVP package proactively for the importer &mdash; saving 6&ndash;12 weeks of import-side documentation work.<\/p>\n<\/div>\n<div class=\"bp-faq\">\n<h3>What is the difference between FDA compliance and PFAS-free certification?<\/h3>\n<p>Two separate frameworks. FDA 21 CFR 176.170 defines acceptable paper components and migration limits. PFAS-free certification (under state bills like CA AB 1200) adds a separate test for organofluorine compounds with thresholds below 100 ppm. A real supplier needs both &mdash; FDA compliance does not automatically include PFAS-free attestation.<\/p>\n<\/div>\n<div class=\"bp-faq\">\n<h3>Can I rely on the The factory&rsquo;s SGS test, or should I commission my own?<\/h3>\n<p>Best practice: trust the This manufacturer&rsquo;s test for ongoing shipments, but commission your own US-based independent test on the first shipment from any new supplier. Cost: $380&ndash;$520. Treat this as supplier qualification cost, not negotiate it away.<\/p>\n<\/div>\n<div class=\"bp-faq\">\n<h3>How often should a real manufacturer re-issue its compliance documentation?<\/h3>\n<p>Migration test: every 12 months and on any silicone or base paper supplier change. PFAS test: every 12 months. FSVP package: annually or on any process change. State PFAS attestation: annually plus on any state bill update. A real A compliant supplier follows this calendar without buyer prompting.<\/p>\n<\/div>\n<div class=\"bp-faq\">\n<h3>What happens if my container is held by CBP for FDA documentation review?<\/h3>\n<p>CBP holds the container pending FDA Office of Compliance review. Detention runs $200&ndash;$350 per day per container. If documentation cannot be produced within 14 days, CBP may issue a refusal of admission and the container ships back to origin at the importer&rsquo;s cost. A real supplier pre-files documentation electronically with the broker on every shipment to prevent this entirely.<\/p>\n<\/div>\n<div class=\"bp-faq\">\n<h3>Can a Chinese The factory maintain FDA compliance over multi-year contracts?<\/h3>\n<p>Yes &mdash; the systems and certifications scale across years and SKUs. The buyer&rsquo;s job is to re-verify documentation freshness annually (request the latest migration test, PFAS test, FSVP package). A serious This manufacturer welcomes this re-verification because it reinforces the buyer&rsquo;s confidence and reduces the buyer&rsquo;s motivation to shop around.<\/p>\n<\/div>\n<div class=\"bp-image\">\n<img decoding=\"async\" src=\"https:\/\/runjiapaper.com\/wp-content\/uploads\/2026\/05\/fda-compliant-manufacturer-fsvp-package-handover-v2-2026.jpg\" alt=\"FDA-compliant manufacturer FSVP package binder handover to US importer compliance officer foodservice paper\"><\/p>\n<div class=\"bp-image-caption\">FSVP package binder handover to US compliance officer at Runjia &mdash; pre-prepared FSMA documentation a real FDA-compliant manufacturer provides upfront.<\/div>\n<\/div>\n<h2>Bottom line for US compliance officers<\/h2>\n<p>If you are auditing an A compliant supplier in 2026, the 9-document checklist is the cheapest insurance you can buy &mdash; 30&ndash;45 minutes of email exchange replaces 6&ndash;14 months of post-shipment compliance firefighting and protects against $24K&ndash;$32K rejection costs per container. A real supplier ships the 9 documents in PDF within 24 hours; a fake one delays, substitutes marketing PDFs, or fails the FDA Industry Systems lookup.<\/p>\n<p>Runjia operates as a registered The factory under FFDCA section 415, with FDA establishment registration number on every 176.170 compliance letter, named silicone supplier (Wacker \/ Dow), state PFAS attestation covering all 5 states, and pre-prepared FSVP packages for every US buyer at no charge.<\/p>\n<div class=\"bp-image\">\n<img decoding=\"async\" src=\"https:\/\/runjiapaper.com\/wp-content\/uploads\/2026\/05\/fda-compliant-manufacturer-5state-pfas-attestation-v2-2026.jpg\" alt=\"FDA-compliant manufacturer state PFAS attestation 5 states CA NY ME WA MN review with US compliance buyers\"><\/p>\n<div class=\"bp-image-caption\">5-state PFAS attestation review (CA \/ NY \/ ME \/ WA \/ MN) with US compliance buyers &mdash; the state-level audit a real FDA-compliant manufacturer covers in one PDF.<\/div>\n<\/div>\n<div class=\"bp-cta\">\n<h2 style=\"margin-top:0;\">Audit Runjia as Your The manufacturer<\/h2>\n<p>Send your audit request. We reply within 24 hours with the full 9-document PDF pack &mdash; FDA establishment registration verified via FDA Industry Systems, state PFAS attestation included.<\/p>\n<p><a class=\"bp-btn\" href=\"#\" onclick=\"elementorProFrontend.modules.popup.showPopup({ id: 5358 }); return false;\">Request a Quote Now<\/a><\/p>\n<div class=\"bp-link-row\">\n<a href=\"mailto:sales4@runjianewmaterial.com\">Email Us<\/a><br \/>\n<a href=\"https:\/\/wa.me\/8619653600360\" target=\"_blank\" rel=\"noopener noreferrer\">Chat on WhatsApp<\/a><br \/>\n<a href=\"https:\/\/runjiapaper.com\/zh\/contact\/\" target=\"_blank\" rel=\"noopener noreferrer\">Contact Page<\/a>\n<\/div>\n<p class=\"bp-note\">FDA registered &middot; FSVP packages prepared &middot; State PFAS attestation 5 states &middot; Wacker\/Dow silicone<\/p>\n<\/div>\n<div class=\"bp-source\">\n<strong>Sources:<\/strong><\/p>\n<ul>\n<li>FDA &mdash; 21 CFR 176.170 Components of Paper and Paperboard in Contact with Aqueous and Fatty Foods<\/li>\n<li>FDA &mdash; FCN Inventory (Food Contact Substance Notifications)<\/li>\n<li>FDA &mdash; FSMA Foreign Supplier Verification Program for Importers of Food<\/li>\n<li>FDA &mdash; Industry Systems Establishment Registration Lookup<\/li>\n<\/ul>\n<\/div>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>FDA-compliant manufacturer audit checklist for 2026 US importers \u2014 9 must-have documents, FDA establishment registration, FSVP package, state PFAS attestation.<\/p>","protected":false},"author":1,"featured_media":7662,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[48,44],"tags":[],"class_list":["post-7524","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-sourcing-import-guides","category-pfas-food-safety-regulation"],"_links":{"self":[{"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/posts\/7524","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/comments?post=7524"}],"version-history":[{"count":5,"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/posts\/7524\/revisions"}],"predecessor-version":[{"id":7664,"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/posts\/7524\/revisions\/7664"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/media\/7662"}],"wp:attachment":[{"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/media?parent=7524"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/categories?post=7524"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/runjiapaper.com\/zh\/wp-json\/wp\/v2\/tags?post=7524"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}