Embotelladoras Autorizado Bajo Lice
FDA import alert and refusal historyCiudad De Mexico, MexicoFEI 3008446507
As of October 26, 2026, Embotelladoras Autorizado Bajo Lice (Ciudad De Mexico, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for be light grapefruit flavored water; be light mango flavored water, published by FDA on May 10, 2012, 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 Embotelladoras Autorizado Bajo Lice
1 record, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 45-02red listBe light Grapefruit flavored water; Be light Mango Flavored WaterSource
Questions about Embotelladoras Autorizado Bajo Lice
- Is Embotelladoras Autorizado Bajo Lice on an FDA import alert?
- Yes. As of October 26, 2026, Embotelladoras Autorizado Bajo Lice is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for be light grapefruit flavored water; be light mango flavored water; FDA published the listing on May 10, 2012.
- Has FDA refused shipments from Embotelladoras Autorizado Bajo Lice?
- No FDA import refusals for Embotelladoras Autorizado Bajo Lice appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Embotelladoras Autorizado Bajo Lice's FEI number?
- Embotelladoras Autorizado Bajo Lice's FDA Establishment Identifier (FEI) is 3008446507.
- Can shipments from Embotelladoras Autorizado Bajo Lice still enter the U.S.?
- Shipments of be light grapefruit flavored water; be light mango flavored water from Embotelladoras Autorizado Bajo Lice 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.