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Luis Alberto Alcaraz Lopez

FDA import alert and refusal historyGuadalajara, MexicoFEI 3001743733

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Example subjectLuis Alberto Alcaraz Lope added to Import Alert 16-129 (red list)

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As of October 26, 2026, Luis Alberto Alcaraz Lopez (Guadalajara, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for lollipop (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 Luis Alberto Alcaraz Lopez

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 listLollipop (without Chocolate)
    Source

Questions about Luis Alberto Alcaraz Lopez

Is Luis Alberto Alcaraz Lopez on an FDA import alert?
Yes. As of October 26, 2026, Luis Alberto Alcaraz Lopez is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for lollipop (without chocolate); FDA published the listing on September 18, 2009.
Has FDA refused shipments from Luis Alberto Alcaraz Lopez?
No FDA import refusals for Luis Alberto Alcaraz Lopez appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Luis Alberto Alcaraz Lopez's FEI number?
Luis Alberto Alcaraz Lopez's FDA Establishment Identifier (FEI) is 3001743733.
Can shipments from Luis Alberto Alcaraz Lopez still enter the U.S.?
Shipments of lollipop (without chocolate) from Luis Alberto Alcaraz Lopez 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 subjectLuis Alberto Alcaraz Lope 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.