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Cesar Alejandro Mena Garcia

FDA import alert and refusal historySan Nicolas De Los Garza, MexicoFEI 2000030419

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Example subjectCesar Alejandro Mena Garci added to Import Alert 16-129 (red list)

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As of October 26, 2026, Cesar Alejandro Mena Garcia (San Nicolas De Los Garza, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh poblano pepper, published by FDA on May 5, 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
None on record

Every FDA record for Cesar Alejandro Mena Garcia

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

2013

  1. Import alert listing
    Listed on Import Alert 99-05red listFresh Poblano Pepper
    Source

Questions about Cesar Alejandro Mena Garcia

Is Cesar Alejandro Mena Garcia on an FDA import alert?
Yes. As of October 26, 2026, Cesar Alejandro Mena Garcia is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh poblano pepper; FDA published the listing on May 5, 2013.
Has FDA refused shipments from Cesar Alejandro Mena Garcia?
No FDA import refusals for Cesar Alejandro Mena Garcia appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Cesar Alejandro Mena Garcia's FEI number?
Cesar Alejandro Mena Garcia's FDA Establishment Identifier (FEI) is 2000030419.
Can shipments from Cesar Alejandro Mena Garcia still enter the U.S.?
Shipments of fresh poblano pepper from Cesar Alejandro Mena Garcia can be detained without physical examination under Import Alert 99-05; 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 subjectCesar Alejandro Mena Garci 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.