Societe Fromagere du Massegros
FDA import alert and refusal historyLe Massegros, FranceFEI 3004295455
Recorded by FDA as SOCIETE FROMAGERE DU MASSEGROS
As of October 26, 2026, Societe Fromagere du Massegros 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 du Massegros
2 records, newest first. Each line links to the FDA page it came from.
2014
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 12-03green listAll soft and soft-ripened cheeses made from sheep's (brebis) milkSource
Questions about Societe Fromagere du Massegros
- Is Societe Fromagere du Massegros on an FDA import alert?
- Yes. As of October 26, 2026, Societe Fromagere du Massegros 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 sheep's (brebis) milk; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Societe Fromagere du Massegros?
- No FDA import refusals for Societe Fromagere du Massegros appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Societe Fromagere du Massegros last inspected by FDA?
- FDA's most recent inspection of Societe Fromagere du Massegros with a final classification is dated March 25, 2014 and was classified NAI (No Action Indicated).
- What is Societe Fromagere du Massegros's FEI number?
- Societe Fromagere du Massegros's FDA Establishment Identifier (FEI) is 3004295455.
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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.