SAS Roque
FDA import alert and refusal historyCollioure, FranceFEI 3011306295
Recorded by FDA as SAS ROQUE
As of October 26, 2026, SAS Roque (Collioure, France) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for ready-to-eat anchovy products, published by FDA on June 5, 2020, 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 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for SAS Roque
2 records, newest first. Each line links to the FDA page it came from.
2020
- Import alert listingListed on Import Alert 16-120red listready-to-eat anchovy productsSource
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about SAS Roque
- Is SAS Roque on an FDA import alert?
- Yes. As of October 26, 2026, SAS Roque is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for ready-to-eat anchovy products; FDA published the listing on June 5, 2020.
- Has FDA refused shipments from SAS Roque?
- No FDA import refusals for SAS Roque appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was SAS Roque last inspected by FDA?
- FDA's most recent inspection of SAS Roque with a final classification is dated February 25, 2020 and was classified OAI (Official Action Indicated).
- What is SAS Roque's FEI number?
- SAS Roque's FDA Establishment Identifier (FEI) is 3011306295.
- Can shipments from SAS Roque still enter the U.S.?
- Shipments of ready-to-eat anchovy products from SAS Roque can be detained without physical examination under Import Alert 16-120; 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.