Oceanside Fish Center Ltd.
FDA import alert and refusal historyPt Cumana, Trinidad and TobagoFEI 3004313130
As of October 26, 2026, Oceanside Fish Center Ltd. (Pt Cumana, Trinidad and Tobago) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for tuna (albacore, yellowfin, bluefin, skipjack, etc.), published by FDA on September 16, 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 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Oceanside Fish Center Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-120red listTuna (Albacore, Yellowfin, Bluefin, Skipjack, Etc.)Source
Questions about Oceanside Fish Center Ltd.
- Is Oceanside Fish Center Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Oceanside Fish Center Ltd. is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for tuna (albacore, yellowfin, bluefin, skipjack, etc.); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Oceanside Fish Center Ltd.?
- No FDA import refusals for Oceanside Fish Center Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Oceanside Fish Center Ltd.'s FEI number?
- Oceanside Fish Center Ltd.'s FDA Establishment Identifier (FEI) is 3004313130.
- Can shipments from Oceanside Fish Center Ltd. still enter the U.S.?
- Shipments of tuna (albacore, yellowfin, bluefin, skipjack, etc.) from Oceanside Fish Center Ltd. 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.