Societe Fromagere de Domfront
FDA import alert and refusal historyDomfront En Poiraie, FranceFEI 3004274099
As of October 26, 2026, Societe Fromagere de Domfront is on the green list of FDA Import Alert 12-03, which exempts its listed products from detention without physical examination under that alert, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 12-03 · green list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Societe Fromagere de Domfront
2 records, newest first. Each line links to the FDA page it came from.
2022
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 12-03green listAll soft and soft-ripened cheeses made from cow's (vache) milkSource
Questions about Societe Fromagere de Domfront
- Is Societe Fromagere de Domfront on an FDA import alert?
- Yes. As of October 26, 2026, Societe Fromagere de Domfront is on the green list of FDA Import Alert 12-03, “Soft and soft-ripened cheese from France”, for all soft and soft-ripened cheeses made from cow's (vache) milk; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Societe Fromagere de Domfront?
- No FDA import refusals for Societe Fromagere de Domfront appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Societe Fromagere de Domfront last inspected by FDA?
- FDA's most recent inspection of Societe Fromagere de Domfront with a final classification is dated December 1, 2022 and was classified NAI (No Action Indicated).
- What is Societe Fromagere de Domfront's FEI number?
- Societe Fromagere de Domfront's FDA Establishment Identifier (FEI) is 3004274099.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.