Centro Internacional de Inversiones, CIISA
FDA import alert and refusal historyLa Ribera De Belen, Costa RicaFEI 3004813380
As of October 26, 2026, Centro Internacional de Inversiones, CIISA (La Ribera De Belen, Costa Rica) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for shrimp, 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 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Centro Internacional de Inversiones, CIISA
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listShrimpSource
Questions about Centro Internacional de Inversiones, CIISA
- Is Centro Internacional de Inversiones, CIISA on an FDA import alert?
- Yes. As of October 26, 2026, Centro Internacional de Inversiones, CIISA is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for shrimp; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Centro Internacional de Inversiones, CIISA?
- No FDA import refusals for Centro Internacional de Inversiones, CIISA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Centro Internacional de Inversiones, CIISA's FEI number?
- Centro Internacional de Inversiones, CIISA's FDA Establishment Identifier (FEI) is 3004813380.
- Can shipments from Centro Internacional de Inversiones, CIISA still enter the U.S.?
- Shipments of shrimp from Centro Internacional de Inversiones, CIISA can be detained without physical examination under Import Alert 16-81; 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.