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Efren Alonso Castro Sandoval

FDA import alert and refusal historyGuadalajara, MexicoFEI 3013031066

Recorded by FDA as EFREN ALONSO CASTRO SANDOVAL

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Example subjectEfren Alonso Castro Sandova added to Import Alert 16-129 (red list)

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As of October 26, 2026, Efren Alonso Castro Sandoval (Guadalajara, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for mango, published by FDA on February 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 Efren Alonso Castro Sandoval

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

2015

  1. Import alert listing
    Listed on Import Alert 99-23red listMango
    Source

Questions about Efren Alonso Castro Sandoval

Is Efren Alonso Castro Sandoval on an FDA import alert?
Yes. As of October 26, 2026, Efren Alonso Castro Sandoval is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for mango; FDA published the listing on February 4, 2015.
Has FDA refused shipments from Efren Alonso Castro Sandoval?
No FDA import refusals for Efren Alonso Castro Sandoval appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Efren Alonso Castro Sandoval's FEI number?
Efren Alonso Castro Sandoval's FDA Establishment Identifier (FEI) is 3013031066.
Can shipments from Efren Alonso Castro Sandoval still enter the U.S.?
Shipments of mango from Efren Alonso Castro Sandoval can be detained without physical examination under Import Alert 99-23; 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 subjectEfren Alonso Castro Sandova 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.