Congeladora de Pescados y Mariscos del Golfo, SA de CV
FDA import alert and refusal historyChampoton, MexicoFEI 3008400120
Recorded by FDA as CONGELADORA DE PESCADOS Y MARISCOS DEL GOLFO, SA DE CV
As of October 27, 2026, Congeladora de Pescados y Mariscos del Golfo, SA de CV (Champoton, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for ladyfish; frozen octopus, published by FDA on April 23, 2015, 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 Congeladora de Pescados y Mariscos del Golfo, SA de CV
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 16-81red listLadyfish; Frozen OctopusSource
Questions about Congeladora de Pescados y Mariscos del Golfo, SA de CV
- Is Congeladora de Pescados y Mariscos del Golfo, SA de CV on an FDA import alert?
- Yes. As of October 27, 2026, Congeladora de Pescados y Mariscos del Golfo, SA de CV is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for ladyfish; frozen octopus; FDA published the listing on April 23, 2015.
- Has FDA refused shipments from Congeladora de Pescados y Mariscos del Golfo, SA de CV?
- No FDA import refusals for Congeladora de Pescados y Mariscos del Golfo, SA de CV appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Congeladora de Pescados y Mariscos del Golfo, SA de CV's FEI number?
- Congeladora de Pescados y Mariscos del Golfo, SA de CV's FDA Establishment Identifier (FEI) is 3008400120.
- Can shipments from Congeladora de Pescados y Mariscos del Golfo, SA de CV still enter the U.S.?
- Shipments of ladyfish; frozen octopus from Congeladora de Pescados y Mariscos del Golfo, SA de CV 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.