Embotelladora de Sidra Pino S. A.
FDA import alert and refusal historyMerida, MexicoFEI 3003741041
As of October 26, 2026, Embotelladora de Sidra Pino S. A. (Merida, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft drink, subtropical or tropical fruit flavored, carbonated; carbonated soft drink, n.e.c., 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 Embotelladora de Sidra Pino S. A.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listSoft Drink, Subtropical or Tropical Fruit Flavored, Carbonated; Carbonated Soft Drink, N.E.C.Source
Questions about Embotelladora de Sidra Pino S. A.
- Is Embotelladora de Sidra Pino S. A. on an FDA import alert?
- Yes. As of October 26, 2026, Embotelladora de Sidra Pino S. A. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft drink, subtropical or tropical fruit flavored, carbonated; carbonated soft drink, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Embotelladora de Sidra Pino S. A.?
- No FDA import refusals for Embotelladora de Sidra Pino S. A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Embotelladora de Sidra Pino S. A.'s FEI number?
- Embotelladora de Sidra Pino S. A.'s FDA Establishment Identifier (FEI) is 3003741041.
- Can shipments from Embotelladora de Sidra Pino S. A. still enter the U.S.?
- Shipments of soft drink, subtropical or tropical fruit flavored, carbonated; carbonated soft drink, n.e.c. from Embotelladora de Sidra Pino S. A. 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.