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Juan Manuel Renteria Salazar

FDA import alert and refusal historyJalpa, MexicoFEI 3010879964

Recorded by FDA as JUAN MANUEL RENTERIA SALAZAR

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Example subjectJuan Manuel Renteria Salaza added to Import Alert 16-129 (red list)

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As of October 26, 2026, Juan Manuel Renteria Salazar (Jalpa, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cactus (nopal), published by FDA on March 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 Juan Manuel Renteria Salazar

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 listCactus (Nopal)
    Source

Questions about Juan Manuel Renteria Salazar

Is Juan Manuel Renteria Salazar on an FDA import alert?
Yes. As of October 26, 2026, Juan Manuel Renteria Salazar is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cactus (nopal); FDA published the listing on March 4, 2015.
Has FDA refused shipments from Juan Manuel Renteria Salazar?
No FDA import refusals for Juan Manuel Renteria Salazar appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Juan Manuel Renteria Salazar's FEI number?
Juan Manuel Renteria Salazar's FDA Establishment Identifier (FEI) is 3010879964.
Can shipments from Juan Manuel Renteria Salazar still enter the U.S.?
Shipments of cactus (nopal) from Juan Manuel Renteria Salazar 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 subjectJuan Manuel Renteria Salaza 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.