Kaisen Co Ltd
FDA import alert and refusal historyFukuoka, JapanFEI 3001837333
As of October 26, 2026, Kaisen Co Ltd (Fukuoka, Japan) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for fish roe, fishery products, n.e.c., 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
- None on record
Every FDA record for Kaisen Co Ltd
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-39red listFish Roe, Fishery Products, n.e.c.Source
Questions about Kaisen Co Ltd
- Is Kaisen Co Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Kaisen Co Ltd is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for fish roe, fishery products, n.e.c.; FDA published the listing on March 13, 2009.
- Has FDA refused shipments from Kaisen Co Ltd?
- No FDA import refusals for Kaisen Co Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kaisen Co Ltd's FEI number?
- Kaisen Co Ltd's FDA Establishment Identifier (FEI) is 3001837333.
- Can shipments from Kaisen Co Ltd still enter the U.S.?
- Shipments of fish roe, fishery products, n.e.c. from Kaisen Co Ltd 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.