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Jorge Ramiro Riestra

FDA import alert and refusal historySonora, MexicoFEI 3001299945

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Example subjectJorge Ramiro Riestr added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jorge Ramiro Riestra (Sonora, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for candy specialties, n.e.c. (without chocolate), published by FDA on September 18, 2009, 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 Ramiro Riestra

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

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listCandy Specialties, N.E.C. (without Chocolate)
    Source

Questions about Jorge Ramiro Riestra

Is Jorge Ramiro Riestra on an FDA import alert?
Yes. As of October 26, 2026, Jorge Ramiro Riestra is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for candy specialties, n.e.c. (without chocolate); FDA published the listing on September 18, 2009.
Has FDA refused shipments from Jorge Ramiro Riestra?
No FDA import refusals for Jorge Ramiro Riestra appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Jorge Ramiro Riestra's FEI number?
Jorge Ramiro Riestra's FDA Establishment Identifier (FEI) is 3001299945.
Can shipments from Jorge Ramiro Riestra still enter the U.S.?
Shipments of candy specialties, n.e.c. (without chocolate) from Jorge Ramiro Riestra can be detained without physical examination under Import Alert 45-02; 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 Ramiro Riestr 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.