L'Epicurien
FDA import alert and refusal historyLe Bosc, FranceFEI 3002663311
As of October 25, 2026, L'Epicurien has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 19, 2017, was classified VAI (Voluntary Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for L'Epicurien
2 records, newest first. Each line links to the FDA page it came from.
Questions about L'Epicurien
- Is L'Epicurien on an FDA import alert?
- No listing for L'Epicurien appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the France page.
- Has FDA refused shipments from L'Epicurien?
- No FDA import refusals for L'Epicurien appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was L'Epicurien last inspected by FDA?
- FDA's most recent inspection of L'Epicurien with a final classification is dated January 19, 2017 and was classified VAI (Voluntary Action Indicated).
- What is L'Epicurien's FEI number?
- L'Epicurien's FDA Establishment Identifier (FEI) is 3002663311.
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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.