Oceaninvest S.A.
FDA import alert and refusal historyGuayaquil, EcuadorFEI 3004256584
As of October 26, 2026, Oceaninvest S.A. (Guayaquil, Ecuador) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for shrimp, published by FDA on November 14, 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 16-81 · 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 Oceaninvest S.A.
2 records, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 16-81red listShrimpSource
2010
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Oceaninvest S.A.
- Is Oceaninvest S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Oceaninvest S.A. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for shrimp; FDA published the listing on November 14, 2012.
- Has FDA refused shipments from Oceaninvest S.A.?
- No FDA import refusals for Oceaninvest S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Oceaninvest S.A. last inspected by FDA?
- FDA's most recent inspection of Oceaninvest S.A. with a final classification is dated May 7, 2010 and was classified OAI (Official Action Indicated).
- What is Oceaninvest S.A.'s FEI number?
- Oceaninvest S.A.'s FDA Establishment Identifier (FEI) is 3004256584.
- Can shipments from Oceaninvest S.A. still enter the U.S.?
- Shipments of shrimp from Oceaninvest 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.