Rompope Coronado Sa De C.V.
FDA import alert and refusal historySan Luis Potosi, MexicoFEI 3011297957
As of October 26, 2026, Rompope Coronado Sa De C.V. (San Luis Potosi, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for sweet goods without custard or cream filling, 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 Rompope Coronado Sa 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 listSweet Goods Without Custard or Cream Filling, N.E.C.Source
Questions about Rompope Coronado Sa De C.V.
- Is Rompope Coronado Sa De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Rompope Coronado Sa De C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sweet goods without custard or cream filling, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Rompope Coronado Sa De C.V.?
- No FDA import refusals for Rompope Coronado Sa De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Rompope Coronado Sa De C.V.'s FEI number?
- Rompope Coronado Sa De C.V.'s FDA Establishment Identifier (FEI) is 3011297957.
- Can shipments from Rompope Coronado Sa De C.V. still enter the U.S.?
- Shipments of sweet goods without custard or cream filling, n.e.c. from Rompope Coronado Sa 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.