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Javier Mejia Alferez Antonio

FDA import alert and refusal historyCiudad De Mexico, MexicoFEI 3010050159

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Example subjectJavier Mejia Alferez Antoni added to Import Alert 16-129 (red list)

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As of October 26, 2026, Javier Mejia Alferez Antonio (Ciudad De Mexico, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for chilaca peppers, published by FDA on March 22, 2016, 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 Javier Mejia Alferez Antonio

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

2016

  1. Import alert listing
    Listed on Import Alert 99-05red listChilaca Peppers
    Source

Questions about Javier Mejia Alferez Antonio

Is Javier Mejia Alferez Antonio on an FDA import alert?
Yes. As of October 26, 2026, Javier Mejia Alferez Antonio is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for chilaca peppers; FDA published the listing on March 22, 2016.
Has FDA refused shipments from Javier Mejia Alferez Antonio?
No FDA import refusals for Javier Mejia Alferez Antonio appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Javier Mejia Alferez Antonio's FEI number?
Javier Mejia Alferez Antonio's FDA Establishment Identifier (FEI) is 3010050159.
Can shipments from Javier Mejia Alferez Antonio still enter the U.S.?
Shipments of chilaca peppers from Javier Mejia Alferez Antonio 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 subjectJavier Mejia Alferez Antoni 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.