Corporacion Del Mar C.A.
FDA import alert and refusal historyMaracaibo, VenezuelaFEI 3004298612
As of October 26, 2026, Corporacion Del Mar C.A. (Maracaibo, Venezuela) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for crabmeat, published by FDA on December 13, 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 Corporacion Del Mar C.A.
2 records, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 16-120red listCrabmeatSource
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Corporacion Del Mar C.A.
- Is Corporacion Del Mar C.A. on an FDA import alert?
- Yes. As of October 26, 2026, Corporacion Del Mar C.A. is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for crabmeat; FDA published the listing on December 13, 2011.
- Has FDA refused shipments from Corporacion Del Mar C.A.?
- No FDA import refusals for Corporacion Del Mar C.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Corporacion Del Mar C.A. last inspected by FDA?
- FDA's most recent inspection of Corporacion Del Mar C.A. with a final classification is dated April 2, 2011 and was classified OAI (Official Action Indicated).
- What is Corporacion Del Mar C.A.'s FEI number?
- Corporacion Del Mar C.A.'s FDA Establishment Identifier (FEI) is 3004298612.
- Can shipments from Corporacion Del Mar C.A. still enter the U.S.?
- Shipments of crabmeat from Corporacion Del Mar C.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.