Gillet
FDA import alert and refusal historyContres, FranceFEI 9888
As of October 25, 2026, Gillet (Contres, France) is on the red list of FDA Import Alert 99-37 (Low-acid canned/acidified foods without scheduled process) for salsify in brine, published by FDA on June 3, 2014, 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 99-37 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Gillet
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-37red listSalsify in brineSource
Questions about Gillet
- Is Gillet on an FDA import alert?
- Yes. As of October 25, 2026, Gillet is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for salsify in brine; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Gillet?
- No FDA import refusals for Gillet appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Gillet's FEI number?
- Gillet's FDA Establishment Identifier (FEI) is 9888.
- Can shipments from Gillet still enter the U.S.?
- Shipments of salsify in brine from Gillet can be detained without physical examination under Import Alert 99-37; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.