Besser Internacional SA de CV
FDA import alert and refusal historyMonterrey, MexicoFEI 3006424328
As of October 26, 2026, Besser Internacional SA de CV (Monterrey, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for chilaca hot; chilaca hot & sour apple paste pineapple flavor; chilaca hot & sour apple paste mango flavor, published by FDA on August 29, 2011, 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
- None on record
Every FDA record for Besser Internacional SA de CV
1 record, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 45-02red listChilaca Hot; Chilaca Hot & Sour Apple Paste Pineapple Flavor; Chilaca Hot & Sour Apple Paste Mango FlavorSource
Questions about Besser Internacional SA de CV
- Is Besser Internacional SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Besser Internacional SA de CV is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for chilaca hot; chilaca hot & sour apple paste pineapple flavor; chilaca hot & sour apple paste mango flavor; FDA published the listing on August 29, 2011.
- Has FDA refused shipments from Besser Internacional SA de CV?
- No FDA import refusals for Besser Internacional SA de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Besser Internacional SA de CV's FEI number?
- Besser Internacional SA de CV's FDA Establishment Identifier (FEI) is 3006424328.
- Can shipments from Besser Internacional SA de CV still enter the U.S.?
- Shipments of chilaca hot; chilaca hot & sour apple paste pineapple flavor; chilaca hot & sour apple paste mango flavor from Besser Internacional SA de CV 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.