Jorge Camacho Valverde
FDA import alert and refusal historySiquirres, Costa RicaFEI 3004310952
As of October 25, 2026, Jorge Camacho Valverde (Siquirres, Costa Rica) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for coriander; culantro, published by FDA on September 7, 2010, 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 99-23 · 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 Jorge Camacho Valverde
2 records, newest first. Each line links to the FDA page it came from.
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2010
- Import alert listingListed on Import Alert 99-23red listCoriander; CulantroSource
Questions about Jorge Camacho Valverde
- Is Jorge Camacho Valverde on an FDA import alert?
- Yes. As of October 25, 2026, Jorge Camacho Valverde is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for coriander; culantro; FDA published the listing on September 7, 2010.
- Has FDA refused shipments from Jorge Camacho Valverde?
- No FDA import refusals for Jorge Camacho Valverde appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Jorge Camacho Valverde last inspected by FDA?
- FDA's most recent inspection of Jorge Camacho Valverde with a final classification is dated November 6, 2012 and was classified VAI (Voluntary Action Indicated).
- What is Jorge Camacho Valverde's FEI number?
- Jorge Camacho Valverde's FDA Establishment Identifier (FEI) is 3004310952.
- Can shipments from Jorge Camacho Valverde still enter the U.S.?
- Shipments of coriander; culantro from Jorge Camacho Valverde can be detained without physical examination under Import Alert 99-23; 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.