Exportadora Interoceanica S A De C V
FDA import alert and refusal historyEnsenada, MexicoFEI 1000428482
As of October 26, 2026, Exportadora Interoceanica S A De C V (Ensenada, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for sand bass; bass, salt or brackisk water (stripe bass, white perch, black bass, etc.), published by FDA on September 18, 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 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Exportadora Interoceanica S A De C V
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listSand bass; Bass, Salt or Brackisk Water (Stripe Bass, white Perch, Black Bass, Etc.)Source
Questions about Exportadora Interoceanica S A De C V
- Is Exportadora Interoceanica S A De C V on an FDA import alert?
- Yes. As of October 26, 2026, Exportadora Interoceanica S A De C V is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for sand bass; bass, salt or brackisk water (stripe bass, white perch, black bass, etc.); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Exportadora Interoceanica S A De C V?
- No FDA import refusals for Exportadora Interoceanica S A De C V appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Exportadora Interoceanica S A De C V's FEI number?
- Exportadora Interoceanica S A De C V's FDA Establishment Identifier (FEI) is 1000428482.
- Can shipments from Exportadora Interoceanica S A De C V still enter the U.S.?
- Shipments of sand bass; bass, salt or brackisk water (stripe bass, white perch, black bass, etc.) from Exportadora Interoceanica S A De C V 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.