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Productos Chata S.A. de C.V.

FDA import alert and refusal historyCuliacan, MexicoFEI 3004272155

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Example subjectProductos Chata S.A. de C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Productos Chata S.A. de C.V. (Culiacan, Mexico) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for tamales (w/sweet corn, published by FDA on October 22, 2019, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Productos Chata S.A. de C.V.

1 record, newest first. Each line links to the FDA page it came from.

2019

  1. Import alert listing
    Listed on Import Alert 99-21red listTamales (w/sweet corn
    Source

Questions about Productos Chata S.A. de C.V.

Is Productos Chata S.A. de C.V. on an FDA import alert?
Yes. As of October 26, 2026, Productos Chata S.A. de C.V. is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for tamales (w/sweet corn; FDA published the listing on October 22, 2019.
Has FDA refused shipments from Productos Chata S.A. de C.V.?
No FDA import refusals for Productos Chata S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Productos Chata S.A. de C.V.'s FEI number?
Productos Chata S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004272155.
Can shipments from Productos Chata S.A. de C.V. still enter the U.S.?
Shipments of tamales (w/sweet corn from Productos Chata S.A. de C.V. can be detained without physical examination under Import Alert 99-21; 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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Example subjectProductos Chata S.A. de C.V added to Import Alert 16-129 (red list)

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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.