Embotelladora Arca S.A. De C.V.
FDA import alert and refusal historyMonterrey, MexicoFEI 3004200829
As of October 26, 2026, Embotelladora Arca S.A. De C.V. (Monterrey, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for fanta orange flavor soft drink; joya brand peach soft drink; joya punch (carbonated soft drink), published by FDA on October 2, 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 Arca 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 listFanta Orange Flavor Soft Drink; Joya Brand Peach Soft Drink; Joya Punch (carbonated soft drink)Source
Questions about Embotelladora Arca S.A. De C.V.
- Is Embotelladora Arca S.A. De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Embotelladora Arca S.A. De C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for fanta orange flavor soft drink; joya brand peach soft drink; joya punch (carbonated soft drink); FDA published the listing on October 2, 2009.
- Has FDA refused shipments from Embotelladora Arca S.A. De C.V.?
- No FDA import refusals for Embotelladora Arca S.A. De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Embotelladora Arca S.A. De C.V.'s FEI number?
- Embotelladora Arca S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3004200829.
- Can shipments from Embotelladora Arca S.A. De C.V. still enter the U.S.?
- Shipments of fanta orange flavor soft drink; joya brand peach soft drink; joya punch (carbonated soft drink) from Embotelladora Arca 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.