Pacific Tropical Fish S.A.
FDA import alert and refusal historyChitre, PanamaFEI 3002736956
As of October 26, 2026, Pacific Tropical Fish S.A. (Chitre, Panama) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for mahi mahi, published by FDA on September 21, 2011, 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 Pacific Tropical Fish S.A.
2 records, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 16-120red listMahi MahiSource
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Pacific Tropical Fish S.A.
- Is Pacific Tropical Fish S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Pacific Tropical Fish S.A. is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for mahi mahi; FDA published the listing on September 21, 2011.
- Has FDA refused shipments from Pacific Tropical Fish S.A.?
- No FDA import refusals for Pacific Tropical Fish S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Pacific Tropical Fish S.A. last inspected by FDA?
- FDA's most recent inspection of Pacific Tropical Fish S.A. with a final classification is dated March 25, 2011 and was classified OAI (Official Action Indicated).
- What is Pacific Tropical Fish S.A.'s FEI number?
- Pacific Tropical Fish S.A.'s FDA Establishment Identifier (FEI) is 3002736956.
- Can shipments from Pacific Tropical Fish S.A. still enter the U.S.?
- Shipments of mahi mahi from Pacific Tropical Fish S.A. 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.