Swg Dominicana, S.A.
FDA import alert and refusal historyLa Ortega Moca, Dominican RepublicFEI 3008247568
As of October 26, 2026, Swg Dominicana, S.A. (La Ortega Moca, Dominican Republic) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for bell peppers; hot peppers, published by FDA on January 27, 2015, 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 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Swg Dominicana, S.A.
3 records, newest first. Each line links to the FDA page it came from.
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2015
- Import alert listingListed on Import Alert 99-05red listBell Peppers; HOT PEPPERSSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Swg Dominicana, S.A.
- Is Swg Dominicana, S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Swg Dominicana, S.A. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for bell peppers; hot peppers; FDA published the listing on January 27, 2015.
- Has FDA refused shipments from Swg Dominicana, S.A.?
- No FDA import refusals for Swg Dominicana, S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Swg Dominicana, S.A. last inspected by FDA?
- FDA's most recent inspection of Swg Dominicana, S.A. with a final classification is dated June 9, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Swg Dominicana, S.A.'s FEI number?
- Swg Dominicana, S.A.'s FDA Establishment Identifier (FEI) is 3008247568.
- Can shipments from Swg Dominicana, S.A. still enter the U.S.?
- Shipments of bell peppers; hot peppers from Swg Dominicana, S.A. can be detained without physical examination under Import Alert 99-05; 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.