Pesquera Isla del Rey S.A
FDA import alert and refusal historyValdivia, ChileFEI 3010227598
Recorded by FDA as PESQUERA ISLA DEL REY S.A
As of October 26, 2026, Pesquera Isla del Rey S.A (Valdivia, Chile) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for crab, published by FDA on March 13, 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 16-39 · 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 Pesquera Isla del Rey S.A
2 records, newest first. Each line links to the FDA page it came from.
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 16-39red listCrabSource
Questions about Pesquera Isla del Rey S.A
- Is Pesquera Isla del Rey S.A on an FDA import alert?
- Yes. As of October 26, 2026, Pesquera Isla del Rey S.A is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for crab; FDA published the listing on March 13, 2009.
- Has FDA refused shipments from Pesquera Isla del Rey S.A?
- No FDA import refusals for Pesquera Isla del Rey S.A appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Pesquera Isla del Rey S.A last inspected by FDA?
- FDA's most recent inspection of Pesquera Isla del Rey S.A with a final classification is dated May 20, 2014 and was classified VAI (Voluntary Action Indicated).
- What is Pesquera Isla del Rey S.A's FEI number?
- Pesquera Isla del Rey S.A's FDA Establishment Identifier (FEI) is 3010227598.
- Can shipments from Pesquera Isla del Rey S.A still enter the U.S.?
- Shipments of crab from Pesquera Isla del Rey S.A can be detained without physical examination under Import Alert 16-39; 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.