Comercializadora de Mariscos Dona Chayo SA de CV
FDA import alert and refusal historyEscuinapa De Hidalgo, MexicoFEI 3011054552
Recorded by FDA as COMERCIALIZADORA DE MARISCOS DONA CHAYO SA DE CV
As of October 27, 2026, Comercializadora de Mariscos Dona Chayo SA de CV (Escuinapa De Hidalgo, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for dry whole shrimp, published by FDA on May 10, 2016, 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 45-02 · 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 Mariscos Dona Chayo SA de CV
1 record, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 45-02red listDry Whole ShrimpSource
Questions about Comercializadora de Mariscos Dona Chayo SA de CV
- Is Comercializadora de Mariscos Dona Chayo SA de CV on an FDA import alert?
- Yes. As of October 27, 2026, Comercializadora de Mariscos Dona Chayo SA de CV is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for dry whole shrimp; FDA published the listing on May 10, 2016.
- Has FDA refused shipments from Comercializadora de Mariscos Dona Chayo SA de CV?
- No FDA import refusals for Comercializadora de Mariscos Dona Chayo SA de CV appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Comercializadora de Mariscos Dona Chayo SA de CV's FEI number?
- Comercializadora de Mariscos Dona Chayo SA de CV's FDA Establishment Identifier (FEI) is 3011054552.
- Can shipments from Comercializadora de Mariscos Dona Chayo SA de CV still enter the U.S.?
- Shipments of dry whole shrimp from Comercializadora de Mariscos Dona Chayo SA de CV can be detained without physical examination under Import Alert 45-02; 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.