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Francisco Armando Gamez Camacho

FDA import alert and refusal historyGonzalez, MexicoFEI 3008617673

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Example subjectFrancisco Armando Gamez Camach added to Import Alert 16-129 (red list)

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As of October 26, 2026, Francisco Armando Gamez Camacho (Gonzalez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for jalapeno pepper, published by FDA on March 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
None on record

Every FDA record for Francisco Armando Gamez Camacho

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 listJalapeno Pepper
    Source

Questions about Francisco Armando Gamez Camacho

Is Francisco Armando Gamez Camacho on an FDA import alert?
Yes. As of October 26, 2026, Francisco Armando Gamez Camacho is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for jalapeno pepper; FDA published the listing on March 26, 2013.
Has FDA refused shipments from Francisco Armando Gamez Camacho?
No FDA import refusals for Francisco Armando Gamez Camacho appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Francisco Armando Gamez Camacho's FEI number?
Francisco Armando Gamez Camacho's FDA Establishment Identifier (FEI) is 3008617673.
Can shipments from Francisco Armando Gamez Camacho still enter the U.S.?
Shipments of jalapeno pepper from Francisco Armando Gamez Camacho 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 subjectFrancisco Armando Gamez Camach 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.