Gabrimar Export Fish S.A.
FDA import alert and refusal historyRemedios, PanamaFEI 3004353769
As of October 26, 2026, Gabrimar Export Fish S.A. (Remedios, 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 February 28, 2012, 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 Gabrimar Export Fish S.A.
2 records, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 16-120red listMahi MahiSource
2011
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Gabrimar Export Fish S.A.
- Is Gabrimar Export Fish S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Gabrimar Export 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 February 28, 2012.
- Has FDA refused shipments from Gabrimar Export Fish S.A.?
- No FDA import refusals for Gabrimar Export Fish S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Gabrimar Export Fish S.A. last inspected by FDA?
- FDA's most recent inspection of Gabrimar Export Fish S.A. with a final classification is dated July 28, 2011 and was classified OAI (Official Action Indicated).
- What is Gabrimar Export Fish S.A.'s FEI number?
- Gabrimar Export Fish S.A.'s FDA Establishment Identifier (FEI) is 3004353769.
- Can shipments from Gabrimar Export Fish S.A. still enter the U.S.?
- Shipments of mahi mahi from Gabrimar Export 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.