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Nazario Gerardo Padilla Manzo

FDA import alert and refusal historyJuarez, MexicoFEI 3010124544

Recorded by FDA as NAZARIO GERARDO PADILLA MANZO

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Example subjectNazario Gerardo Padilla Manz added to Import Alert 16-129 (red list)

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As of October 26, 2026, Nazario Gerardo Padilla Manzo (Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for nopales, published by FDA on February 1, 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 Nazario Gerardo Padilla Manzo

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 listNopales
    Source

Questions about Nazario Gerardo Padilla Manzo

Is Nazario Gerardo Padilla Manzo on an FDA import alert?
Yes. As of October 26, 2026, Nazario Gerardo Padilla Manzo is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for nopales; FDA published the listing on February 1, 2013.
Has FDA refused shipments from Nazario Gerardo Padilla Manzo?
No FDA import refusals for Nazario Gerardo Padilla Manzo appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Nazario Gerardo Padilla Manzo's FEI number?
Nazario Gerardo Padilla Manzo's FDA Establishment Identifier (FEI) is 3010124544.
Can shipments from Nazario Gerardo Padilla Manzo still enter the U.S.?
Shipments of nopales from Nazario Gerardo Padilla Manzo 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 subjectNazario Gerardo Padilla Manz 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.