Mares de Columbia S.A.
FDA import alert and refusal historyGuajira, ColombiaFEI 3000251016
As of October 26, 2026, Mares de Columbia S.A. (Guajira, Colombia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for shrimp & prawns; shrimp and prawns, aquaculture harvested fishery/seafood products, published by FDA on September 18, 2009, 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 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Mares de Columbia S.A.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listShrimp & Prawns; Shrimp and prawns, Aquaculture Harvested Fishery/Seafood ProductsSource
Questions about Mares de Columbia S.A.
- Is Mares de Columbia S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Mares de Columbia S.A. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for shrimp & prawns; shrimp and prawns, aquaculture harvested fishery/seafood products; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Mares de Columbia S.A.?
- No FDA import refusals for Mares de Columbia S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Mares de Columbia S.A.'s FEI number?
- Mares de Columbia S.A.'s FDA Establishment Identifier (FEI) is 3000251016.
- Can shipments from Mares de Columbia S.A. still enter the U.S.?
- Shipments of shrimp & prawns; shrimp and prawns, aquaculture harvested fishery/seafood products from Mares de Columbia S.A. can be detained without physical examination under Import Alert 16-81; 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.