C.I. Vegetales Sorrento Ltda.
FDA import alert and refusal historyRicaurte, ColombiaFEI 3006782518
As of October 26, 2026, C.I. Vegetales Sorrento Ltda. (Ricaurte, Colombia) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for basil (albahaca), 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 C.I. Vegetales Sorrento Ltda.
2 records, newest first. Each line links to the FDA page it came from.
2010
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 99-23red listBasil (Albahaca)Source
Questions about C.I. Vegetales Sorrento Ltda.
- Is C.I. Vegetales Sorrento Ltda. on an FDA import alert?
- Yes. As of October 26, 2026, C.I. Vegetales Sorrento Ltda. is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for basil (albahaca); FDA published the listing on September 7, 2010.
- Has FDA refused shipments from C.I. Vegetales Sorrento Ltda.?
- No FDA import refusals for C.I. Vegetales Sorrento Ltda. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was C.I. Vegetales Sorrento Ltda. last inspected by FDA?
- FDA's most recent inspection of C.I. Vegetales Sorrento Ltda. with a final classification is dated December 17, 2010 and was classified VAI (Voluntary Action Indicated).
- What is C.I. Vegetales Sorrento Ltda.'s FEI number?
- C.I. Vegetales Sorrento Ltda.'s FDA Establishment Identifier (FEI) is 3006782518.
- Can shipments from C.I. Vegetales Sorrento Ltda. still enter the U.S.?
- Shipments of basil (albahaca) from C.I. Vegetales Sorrento Ltda. 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.