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Ets Mandiang & Freres Sarl

FDA import alert and refusal historyDakar, SenegalFEI 3010614401

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Example subjectEts Mandiang & Freres Sar added to Import Alert 16-129 (red list)

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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

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

  1. Import alert listing
    Listed on Import Alert 16-120red listAll fishery products
    Source
  2. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

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.