Ets Mandiang & Freres Sarl
FDA import alert and refusal historyDakar, SenegalFEI 3010614401
As of October 26, 2026, Ets Mandiang & Freres Sarl (Dakar, Senegal) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for all fishery products, published by FDA on September 16, 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 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 Ets Mandiang & Freres Sarl
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 16-120red listAll fishery productsSource
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Ets Mandiang & Freres Sarl
- Is Ets Mandiang & Freres Sarl on an FDA import alert?
- Yes. As of October 26, 2026, Ets Mandiang & Freres Sarl is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for all fishery products; FDA published the listing on September 16, 2014.
- Has FDA refused shipments from Ets Mandiang & Freres Sarl?
- No FDA import refusals for Ets Mandiang & Freres Sarl appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Ets Mandiang & Freres Sarl last inspected by FDA?
- FDA's most recent inspection of Ets Mandiang & Freres Sarl with a final classification is dated January 21, 2014 and was classified OAI (Official Action Indicated).
- What is Ets Mandiang & Freres Sarl's FEI number?
- Ets Mandiang & Freres Sarl's FDA Establishment Identifier (FEI) is 3010614401.
- Can shipments from Ets Mandiang & Freres Sarl still enter the U.S.?
- Shipments of all fishery products from Ets Mandiang & Freres Sarl 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.