Embotelladora Aga Del
FDA import alert and refusal historyQueretaro, MexicoFEI 3003557696
As of October 25, 2026, Embotelladora Aga Del (Queretaro, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft drink, citrus 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 Aga Del
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, Citrus Fruit Flavored, Carbonated; Carbonated Soft Drink, N.E.C.Source
Questions about Embotelladora Aga Del
- Is Embotelladora Aga Del on an FDA import alert?
- Yes. As of October 25, 2026, Embotelladora Aga Del is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft drink, citrus fruit flavored, carbonated; carbonated soft drink, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Embotelladora Aga Del?
- No FDA import refusals for Embotelladora Aga Del appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Embotelladora Aga Del's FEI number?
- Embotelladora Aga Del's FDA Establishment Identifier (FEI) is 3003557696.
- Can shipments from Embotelladora Aga Del still enter the U.S.?
- Shipments of soft drink, citrus fruit flavored, carbonated; carbonated soft drink, n.e.c. from Embotelladora Aga Del 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.