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Minsa S.A. de C.V.

FDA import alert and refusal historyTlalnepantla de Baz, MexicoFEI 3003166909

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

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As of October 26, 2026, Minsa S.A. de C.V. (Tlalnepantla de Baz, Mexico) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for extra white corn flour, published by FDA on July 26, 2013, 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
Classified NAI (No Action Indicated)

Every FDA record for Minsa S.A. de C.V.

2 records, newest first. Each line links to the FDA page it came from.

2014

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2013

  1. Import alert listing
    Listed on Import Alert 99-08red listExtra White Corn Flour
    Source

Questions about Minsa S.A. de C.V.

Is Minsa S.A. de C.V. on an FDA import alert?
Yes. As of October 26, 2026, Minsa S.A. de C.V. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for extra white corn flour; FDA published the listing on July 26, 2013.
Has FDA refused shipments from Minsa S.A. de C.V.?
No FDA import refusals for Minsa S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Minsa S.A. de C.V. last inspected by FDA?
FDA's most recent inspection of Minsa S.A. de C.V. with a final classification is dated October 14, 2014 and was classified NAI (No Action Indicated).
What is Minsa S.A. de C.V.'s FEI number?
Minsa S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3003166909.
Can shipments from Minsa S.A. de C.V. still enter the U.S.?
Shipments of extra white corn flour from Minsa S.A. de C.V. can be detained without physical examination under Import Alert 99-08; 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.