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Juan Antonio Castelo De la Rosa

FDA import alert and refusal historyMiguel Aleman De La Doce, MexicoFEI 3009972596

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Example subjectJuan Antonio Castelo De la Ros added to Import Alert 16-129 (red list)

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As of October 26, 2026, Juan Antonio Castelo De la Rosa (Miguel Aleman De La Doce, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for yellow pepper, published by FDA on March 29, 2013, 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 Antonio Castelo De la Rosa

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

2013

  1. Import alert listing
    Listed on Import Alert 99-05red listYellow Pepper
    Source

Questions about Juan Antonio Castelo De la Rosa

Is Juan Antonio Castelo De la Rosa on an FDA import alert?
Yes. As of October 26, 2026, Juan Antonio Castelo De la Rosa is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for yellow pepper; FDA published the listing on March 29, 2013.
Has FDA refused shipments from Juan Antonio Castelo De la Rosa?
No FDA import refusals for Juan Antonio Castelo De la Rosa appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Juan Antonio Castelo De la Rosa's FEI number?
Juan Antonio Castelo De la Rosa's FDA Establishment Identifier (FEI) is 3009972596.
Can shipments from Juan Antonio Castelo De la Rosa still enter the U.S.?
Shipments of yellow pepper from Juan Antonio Castelo De la Rosa 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 Antonio Castelo De la Ros 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.