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Jorge Alejandro Ornelas Torres

FDA import alert and refusal historyTaretan, MexicoFEI 3011656443

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Example subjectJorge Alejandro Ornelas Torre added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jorge Alejandro Ornelas Torres (Taretan, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh guavas, published by FDA on November 4, 2015, 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 Alejandro Ornelas Torres

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

2015

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

Questions about Jorge Alejandro Ornelas Torres

Is Jorge Alejandro Ornelas Torres on an FDA import alert?
Yes. As of October 26, 2026, Jorge Alejandro Ornelas Torres is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh guavas; FDA published the listing on November 4, 2015.
Has FDA refused shipments from Jorge Alejandro Ornelas Torres?
No FDA import refusals for Jorge Alejandro Ornelas Torres appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Jorge Alejandro Ornelas Torres's FEI number?
Jorge Alejandro Ornelas Torres's FDA Establishment Identifier (FEI) is 3011656443.
Can shipments from Jorge Alejandro Ornelas Torres still enter the U.S.?
Shipments of fresh guavas from Jorge Alejandro Ornelas Torres 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 Alejandro Ornelas Torre 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.