Sushi Den Japan
FDA import alert and refusal historyFukuoka, JapanFEI 3010125085
Recorded by FDA as SUSHI DEN JAPAN
As of October 26, 2026, Sushi Den Japan (Fukuoka, Japan) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for bonita; spanish mackerel; jack mackerel; yellowtail, published by FDA on August 26, 2014, 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 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Sushi Den Japan
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 16-120red listBonita; Spanish Mackerel; Jack Mackerel; YellowtailSource
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Sushi Den Japan
- Is Sushi Den Japan on an FDA import alert?
- Yes. As of October 26, 2026, Sushi Den Japan is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for bonita; spanish mackerel; jack mackerel; yellowtail; FDA published the listing on August 26, 2014.
- Has FDA refused shipments from Sushi Den Japan?
- No FDA import refusals for Sushi Den Japan appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Sushi Den Japan last inspected by FDA?
- FDA's most recent inspection of Sushi Den Japan with a final classification is dated February 6, 2014 and was classified OAI (Official Action Indicated).
- What is Sushi Den Japan's FEI number?
- Sushi Den Japan's FDA Establishment Identifier (FEI) is 3010125085.
- Can shipments from Sushi Den Japan still enter the U.S.?
- Shipments of bonita; spanish mackerel; jack mackerel; yellowtail from Sushi Den Japan can be detained without physical examination under Import Alert 16-120; 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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