If you are importing pet food for the first time, the registration maze is usually the least understood part of the project — and the one that causes the most surprises at customs. This article explains the two most common destination markets (United States and European Union), who is responsible for what, and the mistakes we see importers make repeatedly.

A good rule of thumb: the factory holds the export-side registrations; the importer owns destination-market compliance. Both sides failing to understand this boundary is how shipments get held.

United States: FDA facility registration

What must be registered

Under the FDA's food facility registration requirements (rooted in FSMA, with preventive-control rules at 21 CFR Part 507), any facility that manufactures, processes, packs or holds pet food for sale in the US must be registered with the FDA. This applies to the foreign manufacturing facility — not just the US importer. Registration is not a one-time event: it must be renewed every two years, and the renewal period is an official window each even-numbered year.

What the factory needs

What the importer must also handle

The registration belongs to the factory, but the import entry is yours. Practical items that stop shipments: accurate product labels consistent with AAFCO model regulations, an FDA Prior Notice filed before arrival, and — increasingly — documentation readiness if your product is selected for examination. Most importers work with a customs broker for entry and a regulatory specialist for label review.

European Union: establishment approval and import checks

Two different EU regimes

Pet food in the EU is regulated partly as feed and partly under animal-by-product rules, so "EU registration" is not a single certificate. The key pieces for imported pet food:

The common trap

EU requirements differ by product type — a freeze-dried treat containing animal protein is not treated identically to a fully plant-based supplement. Importers often discover this only after ordering, when the factory says "we export to the EU" but cannot show which product categories their approval covers. Ask the factory for the exact product scope of their approval, in writing, before you commit.

Who does what — a simple division

ResponsibilityFactory (exporter)You (importer)
Facility registration / establishment approvalHolds and maintains itVerifies it, checks renewal dates
Label compliance for destination marketOften assists / reviewsFinal responsibility
Import entry & customs filingProvides documents (invoice, COA, health certs)Files via broker / handles prior notice
Batch testing & COAProvides per-batchRequests destination-market tests if needed
Traceability & recallMaintains production recordsMaintains distribution records

Five mistakes that stop shipments

  1. "They have ISO, so the US is fine." ISO 22000 is a management system; FDA registration is a legal requirement. They are different documents.
  2. Expired registration numbers. The renewal window comes around every two years; an expired FFR number is caught at import.
  3. Label vs. registration mismatch. The product name and ingredients on the label must match what the facility is registered and approved to produce.
  4. Assuming the factory handles destination-market compliance. Most factories handle export side; importers must own the destination side. Confirm the split before the PO.
  5. Only asking "do you export to the US/EU?" Ask: to which markets in the last 12 months, with which product categories, and can you show the documents?

What a compliant supplier looks like

A serious pet food exporter answers registration questions in the first call, sends the registration numbers and renewal dates as a follow-up email the same day, and states plainly which product categories their approvals cover. They also tell you what you still need to do — because they have done this many times and know the boundary between their paperwork and yours. That clarity is worth more than a slightly lower price.

This article is a general orientation, not legal or regulatory advice. Requirements change: always verify against official FDA and EU regulator information, and involve a qualified customs/regulatory professional for your specific products and markets.