Frudest, S.A. de C.V.
FDA import alert and refusal historyTlaquepaque, MexicoFEI 3004815286
As of October 26, 2026, Frudest, S.A. de C.V. (Tlaquepaque, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for chilimon, published by FDA on April 23, 2013, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Frudest, S.A. de C.V.
2 records, newest first. Each line links to the FDA page it came from.
2020
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2013
- Import alert listingListed on Import Alert 45-02red listChilimonSource
Questions about Frudest, S.A. de C.V.
- Is Frudest, S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Frudest, S.A. de C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for chilimon; FDA published the listing on April 23, 2013.
- Has FDA refused shipments from Frudest, S.A. de C.V.?
- No FDA import refusals for Frudest, S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Frudest, S.A. de C.V. last inspected by FDA?
- FDA's most recent inspection of Frudest, S.A. de C.V. with a final classification is dated January 9, 2020 and was classified VAI (Voluntary Action Indicated).
- What is Frudest, S.A. de C.V.'s FEI number?
- Frudest, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004815286.
- Can shipments from Frudest, S.A. de C.V. still enter the U.S.?
- Shipments of chilimon from Frudest, S.A. de C.V. 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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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.