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SUSHI DEN JAPAN FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Latest inspection OAI · Feb 6, 2014
Last warning letter 2014

Inspections 1

1 OAI

Recalls 0 0 Class I

Warning letters 1 Latest Jun 24, 2014

510(k) clearances 0 None on file

SUSHI DEN JAPAN has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to SUSHI DEN JAPAN, the most recent on Jun 24, 2014.

What these totals cover: FDA records filed under the name "SUSHI DEN JAPAN".

Latest inspection: Feb 6, 2014 · OAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	1	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

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SUSHI DEN JAPAN FDA Warning Letters

1 warning letter on Jun 24, 2014.

Issued	Subject	Issuing office	Close-out letter
Jun 24, 2014 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

1 inspection on Feb 6, 2014.

Date	Site	Product	Classification	FEI
Feb 6, 2014	Fukuoka, Japan	Food/Cosmetics	Official Action Indicated (OAI)	3010125085

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under SUSHI DEN JAPAN: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jun 24, 2014.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3010125085	Fukuoka, Japan	1	Feb 6, 2014

SUSHI DEN JAPAN and the FDA: common questions

Has SUSHI DEN JAPAN received an FDA warning letter?

Yes. FDA has issued 1 warning letter to SUSHI DEN JAPAN. The most recent is dated Jun 24, 2014.

Has SUSHI DEN JAPAN received an FDA Form 483?

FDA has not published a Form 483 for "SUSHI DEN JAPAN" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect SUSHI DEN JAPAN?

The most recent FDA inspection on file ended Feb 6, 2014 at Fukuoka, Japan and was classified OAI. FDA has 1 inspection of SUSHI DEN JAPAN on file, 1 of them classified OAI (official action indicated).

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