FDA / FSMA pathway
Project review covers the animal-food facility route, label and ingredient declarations, import documentation and the applicable food-safety plan.
Pet Food OEM Quality & Compliance
Check production conditions, labels and export documents against the destination market.
At project intake, Aumeats confirms the proposed formula, selected production base, destination market and importer requirements, then coordinates the applicable compliance-document checklist.
Quality and compliance
How are quality and destination-market requirements reviewed?
A project-specific checklist links the proposed product, legal manufacturing entity and destination market. It can cover ingredient information, process controls, testing, traceability, specifications, labels, certificates, registrations and export documents. Displayed facility documents support preliminary qualification only; their issuer, named entity, site, product scope, validity and current status must be checked. Certification does not by itself establish product approval or import eligibility. Final legal and market decisions remain with the importer and qualified destination-market advisers under current requirements.
Feed Law / ABP / TRACES
Planning addresses feed hygiene, animal by-products, required label languages and the relevant import-document route.
DAFF / MPI
Destination requirements, heat treatment, ingredient restrictions, certificates and clearance documents are checked for the proposed product.
HACCP / ISO / Facility Files
The selected manufacturing entity's current systems, certificate scope and validity are reviewed, with order-specific batch documents agreed separately.
Claims & Labelling
Ingredient lists, nutritional declarations, feeding directions, origin, barcodes, warnings and required language versions are coordinated within the agreed responsibility matrix.
COA / Invoice / Packing List
The project pack may include a COA, commercial invoice, packing list, origin document, health document, test reports and clearance records where applicable.
Market access depends on the formula, manufacturing process, selected legal manufacturing entity, current certificate scope and importer requirements. Aumeats verifies these factors before quotation confirmation and commercial production; this general overview does not replace a product-specific regulatory review.
Quality Control Workflow
Controls cover raw materials, production, testing, documentation and shipment release.
Supplier and material approval
Review material origin, specification, batch documents, higher-risk inputs and destination restrictions.
Maintain the applicable material file, approved-supplier list and substitution controls.
Sample and formula confirmation
Confirm analytical targets, palatability, texture, moisture, dimensions, packaging and label direction.
Retain controlled sample versions, formula versions and written customer approvals.
Production-process control
Monitor weighing, forming, drying or thermal treatment, metal detection, packing, retention samples and batch traceability as applicable.
Maintain production, deviation and in-process inspection records.
Finished-product testing and release
Check moisture, microbiology, sensory attributes, net content and seal integrity according to the product and market plan.
Coordinate the agreed COA, test report, retention record and release confirmation.
Export documentation
Prepare the commercial invoice, packing list, COA, origin, health or veterinary documents, labels and clearance records where applicable.
Add importer-, platform- or destination-specific files only where confirmed for the project.