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Jorge Antonio Garcia Sanchez

FDA import alert and refusal historyMexico, MexicoFEI 3004699774

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Example subjectJorge Antonio Garcia Sanche added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jorge Antonio Garcia Sanchez (Mexico, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for papayas (papaw fresh); papaya, published by FDA on December 8, 2011, 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 Jorge Antonio Garcia Sanchez

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

2011

  1. Import alert listing
    Listed on Import Alert 99-05red listPapayas (Papaw Fresh); Papaya
    Source

Questions about Jorge Antonio Garcia Sanchez

Is Jorge Antonio Garcia Sanchez on an FDA import alert?
Yes. As of October 26, 2026, Jorge Antonio Garcia Sanchez is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for papayas (papaw fresh); papaya; FDA published the listing on December 8, 2011.
Has FDA refused shipments from Jorge Antonio Garcia Sanchez?
No FDA import refusals for Jorge Antonio Garcia Sanchez appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Jorge Antonio Garcia Sanchez's FEI number?
Jorge Antonio Garcia Sanchez's FDA Establishment Identifier (FEI) is 3004699774.
Can shipments from Jorge Antonio Garcia Sanchez still enter the U.S.?
Shipments of papayas (papaw fresh); papaya from Jorge Antonio Garcia Sanchez 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 subjectJorge Antonio Garcia Sanche 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.