Perrin-Vermot SA
FDA import alert and refusal historyCleron, FranceFEI 3004262148
As of October 26, 2026, Perrin-Vermot SA 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 Perrin-Vermot SA
3 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2014
- Import alert listingListed on Import Alert 12-03green listAll soft and soft-ripened cheeses made from cow's (vache) milkSource
2012
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Perrin-Vermot SA
- Is Perrin-Vermot SA on an FDA import alert?
- Yes. As of October 26, 2026, Perrin-Vermot SA 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 July 11, 2014.
- Has FDA refused shipments from Perrin-Vermot SA?
- No FDA import refusals for Perrin-Vermot SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Perrin-Vermot SA last inspected by FDA?
- FDA's most recent inspection of Perrin-Vermot SA with a final classification is dated September 10, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Perrin-Vermot SA's FEI number?
- Perrin-Vermot SA's FDA Establishment Identifier (FEI) is 3004262148.
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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.