Grupo Tampico Sa De Cv
FDA import alert and refusal historyTampico, MexicoFEI 3005233759
As of October 26, 2026, Grupo Tampico Sa De Cv (Tampico, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for strawberry flavored soft drink (escuis brand); orange flavored drink escuis brand; fanta orange soft drink; fanta orange soft drink, 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
- 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 Grupo Tampico Sa De Cv
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listStrawberry Flavored Soft Drink (Escuis Brand); Orange flavored drink Escuis Brand; Fanta orange soft drink; Fanta Orange Soft DrinkSource
Questions about Grupo Tampico Sa De Cv
- Is Grupo Tampico Sa De Cv on an FDA import alert?
- Yes. As of October 26, 2026, Grupo Tampico Sa De Cv is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for strawberry flavored soft drink (escuis brand); orange flavored drink escuis brand; fanta orange soft drink; fanta orange soft drink; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Grupo Tampico Sa De Cv?
- No FDA import refusals for Grupo Tampico Sa De Cv appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Grupo Tampico Sa De Cv's FEI number?
- Grupo Tampico Sa De Cv's FDA Establishment Identifier (FEI) is 3005233759.
- Can shipments from Grupo Tampico Sa De Cv still enter the U.S.?
- Shipments of strawberry flavored soft drink (escuis brand); orange flavored drink escuis brand; fanta orange soft drink; fanta orange soft drink from Grupo Tampico 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.