Centro Dominicano De Promocion De
FDA import alert and refusal historySanto Domingo De Guzman, Dominican RepublicFEI 1000290693
As of October 26, 2026, Centro Dominicano De Promocion De (Santo Domingo De Guzman, Dominican Republic) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for quisquella vanilla, published by FDA on March 2, 2023, 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 99-45 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Centro Dominicano De Promocion De
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 99-45red listQuisquella VanillaSource
Questions about Centro Dominicano De Promocion De
- Is Centro Dominicano De Promocion De on an FDA import alert?
- Yes. As of October 26, 2026, Centro Dominicano De Promocion De is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for quisquella vanilla; FDA published the listing on March 2, 2023.
- Has FDA refused shipments from Centro Dominicano De Promocion De?
- No FDA import refusals for Centro Dominicano De Promocion De appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Centro Dominicano De Promocion De's FEI number?
- Centro Dominicano De Promocion De's FDA Establishment Identifier (FEI) is 1000290693.
- Can shipments from Centro Dominicano De Promocion De still enter the U.S.?
- Shipments of quisquella vanilla from Centro Dominicano De Promocion De can be detained without physical examination under Import Alert 99-45; 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.