Gebroeders Kooy B.V.
FDA import alert and refusal historyHuizen, NetherlandsFEI 3004277663
As of October 26, 2026, Gebroeders Kooy B.V. (Huizen, Netherlands) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for frozen cold smoked halibut, published by FDA on July 2, 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 16-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Gebroeders Kooy B.V.
2 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2015
- Import alert listingListed on Import Alert 16-39red listFrozen Cold Smoked HalibutSource
Questions about Gebroeders Kooy B.V.
- Is Gebroeders Kooy B.V. on an FDA import alert?
- Yes. As of October 26, 2026, Gebroeders Kooy B.V. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for frozen cold smoked halibut; FDA published the listing on July 2, 2015.
- Has FDA refused shipments from Gebroeders Kooy B.V.?
- No FDA import refusals for Gebroeders Kooy B.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Gebroeders Kooy B.V. last inspected by FDA?
- FDA's most recent inspection of Gebroeders Kooy B.V. with a final classification is dated May 16, 2018 and was classified NAI (No Action Indicated).
- What is Gebroeders Kooy B.V.'s FEI number?
- Gebroeders Kooy B.V.'s FDA Establishment Identifier (FEI) is 3004277663.
- Can shipments from Gebroeders Kooy B.V. still enter the U.S.?
- Shipments of frozen cold smoked halibut from Gebroeders Kooy B.V. 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.