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Ribon Company, Ltd. FDA Record

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

Ribon Company, Ltd. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Ribon Company, Ltd., the most recent on Oct 5, 2015.

What these totals cover: FDA records filed under the name "Ribon Company, Ltd." and its spelling variant "Ribon Company".

Latest inspection: Feb 8, 2019 · NAI

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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	2	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

Ribon Company, Ltd. FDA Warning Letters

1 warning letter on Oct 5, 2015.

Issued	Subject	Issuing office	Close-out letter
Oct 5, 2015

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

2 inspections from Feb 20, 2015 to Feb 8, 2019.

Date	Site	Product	Classification	FEI
Feb 8, 2019	Komaki, Japan	Food/Cosmetics	No Action Indicated (NAI)	3010493762
Feb 20, 2015	Komaki, Japan	Food/Cosmetics	Official Action Indicated (OAI)	3010493762

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 Ribon Company, Ltd.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Oct 5, 2015.

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 3010493762	Komaki, Japan	2	Feb 8, 2019

Ribon Company, Ltd. and the FDA: common questions

Has Ribon Company, Ltd. received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Ribon Company, Ltd.. The most recent is dated Oct 5, 2015.

Has Ribon Company, Ltd. received an FDA Form 483?

FDA has not published a Form 483 for "Ribon Company, Ltd." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Ribon Company, Ltd.?

The most recent FDA inspection on file ended Feb 8, 2019 at Komaki, Japan and was classified NAI. FDA has 2 inspections of Ribon Company, Ltd. on file, 1 of them classified OAI (official action indicated).

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