Fromagerie De L'Ermitage
FDA import alert and refusal historyBulgneville, FranceFEI 3004287243
As of October 25, 2026, Fromagerie De L'Ermitage 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 VAI (Voluntary Action Indicated)
Every FDA record for Fromagerie De L'Ermitage
3 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2011
- 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 cows (vache) milkSource
Questions about Fromagerie De L'Ermitage
- Is Fromagerie De L'Ermitage on an FDA import alert?
- Yes. As of October 25, 2026, Fromagerie De L'Ermitage 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 cows (vache) milk; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Fromagerie De L'Ermitage?
- No FDA import refusals for Fromagerie De L'Ermitage appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Fromagerie De L'Ermitage last inspected by FDA?
- FDA's most recent inspection of Fromagerie De L'Ermitage with a final classification is dated April 13, 2018 and was classified VAI (Voluntary Action Indicated).
- What is Fromagerie De L'Ermitage's FEI number?
- Fromagerie De L'Ermitage's FDA Establishment Identifier (FEI) is 3004287243.
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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.