Green Bay International, S.A.
FDA import alert and refusal historyDavid, PanamaFEI 3005113672
As of October 26, 2026, Green Bay International, S.A. (David, Panama) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for wahoo, published by FDA on December 14, 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 Green Bay International, 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 listWahooSource
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Green Bay International, S.A.
- Is Green Bay International, S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Green Bay International, S.A. is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for wahoo; FDA published the listing on December 14, 2011.
- Has FDA refused shipments from Green Bay International, S.A.?
- No FDA import refusals for Green Bay International, S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Green Bay International, S.A. last inspected by FDA?
- FDA's most recent inspection of Green Bay International, S.A. with a final classification is dated July 26, 2011 and was classified OAI (Official Action Indicated).
- What is Green Bay International, S.A.'s FEI number?
- Green Bay International, S.A.'s FDA Establishment Identifier (FEI) is 3005113672.
- Can shipments from Green Bay International, S.A. still enter the U.S.?
- Shipments of wahoo from Green Bay International, 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.