Comercializadora de Productos Marinos (Compromar)
FDA import alert and refusal historyMaracaibo, VenezuelaFEI 2000014539
As of October 26, 2026, Comercializadora de Productos Marinos (Compromar) (Maracaibo, Venezuela) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for crabmeat; pasteurized and unpasteurized, published by FDA on April 19, 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 16-105 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Comercializadora de Productos Marinos (Compromar)
1 record, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 16-105red listCrabmeat; pasteurized and unpasteurizedSource
Questions about Comercializadora de Productos Marinos (Compromar)
- Is Comercializadora de Productos Marinos (Compromar) on an FDA import alert?
- Yes. As of October 26, 2026, Comercializadora de Productos Marinos (Compromar) is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for crabmeat; pasteurized and unpasteurized; FDA published the listing on April 19, 2011.
- Has FDA refused shipments from Comercializadora de Productos Marinos (Compromar)?
- No FDA import refusals for Comercializadora de Productos Marinos (Compromar) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Comercializadora de Productos Marinos (Compromar)'s FEI number?
- Comercializadora de Productos Marinos (Compromar)'s FDA Establishment Identifier (FEI) is 2000014539.
- Can shipments from Comercializadora de Productos Marinos (Compromar) still enter the U.S.?
- Shipments of crabmeat; pasteurized and unpasteurized from Comercializadora de Productos Marinos (Compromar) can be detained without physical examination under Import Alert 16-105; 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.