Manantiales Penafiel, S.A De C.V.
FDA import alert and refusal historyMexico, D.F., MexicoFEI 1000564721
As of October 26, 2026, Manantiales Penafiel, S.A De C.V. (Mexico, D.F., Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for sangria flavored soft drink; strawberry flavored carbonated mineral water, 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 Manantiales Penafiel, S.A De C.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listsangria flavored soft drink; strawberry flavored carbonated mineral waterSource
Questions about Manantiales Penafiel, S.A De C.V.
- Is Manantiales Penafiel, S.A De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Manantiales Penafiel, S.A De C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sangria flavored soft drink; strawberry flavored carbonated mineral water; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Manantiales Penafiel, S.A De C.V.?
- No FDA import refusals for Manantiales Penafiel, S.A De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Manantiales Penafiel, S.A De C.V.'s FEI number?
- Manantiales Penafiel, S.A De C.V.'s FDA Establishment Identifier (FEI) is 1000564721.
- Can shipments from Manantiales Penafiel, S.A De C.V. still enter the U.S.?
- Shipments of sangria flavored soft drink; strawberry flavored carbonated mineral water from Manantiales Penafiel, 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.