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Leopoldo Garcia Velazquez

FDA import alert and refusal historyEnsenada, MexicoFEI 3011023476

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Example subjectLeopoldo Garcia Velazque added to Import Alert 16-129 (red list)

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As of October 26, 2026, Leopoldo Garcia Velazquez (Ensenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for mexican squash (tatuma; summer squash), published by FDA on January 13, 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 Leopoldo Garcia Velazquez

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 listMexican Squash (Tatuma; summer squash)
    Source

Questions about Leopoldo Garcia Velazquez

Is Leopoldo Garcia Velazquez on an FDA import alert?
Yes. As of October 26, 2026, Leopoldo Garcia Velazquez is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for mexican squash (tatuma; summer squash); FDA published the listing on January 13, 2015.
Has FDA refused shipments from Leopoldo Garcia Velazquez?
No FDA import refusals for Leopoldo Garcia Velazquez appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Leopoldo Garcia Velazquez's FEI number?
Leopoldo Garcia Velazquez's FDA Establishment Identifier (FEI) is 3011023476.
Can shipments from Leopoldo Garcia Velazquez still enter the U.S.?
Shipments of mexican squash (tatuma; summer squash) from Leopoldo Garcia Velazquez 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 subjectLeopoldo Garcia Velazque 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.