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Yamahide Shokuhin, Inc. FDA Record

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

Yamahide Shokuhin, Inc. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Yamahide Shokuhin, Inc., the most recent on Dec 30, 2014.

What these totals cover: FDA records filed under the name "Yamahide Shokuhin, Inc." and its spelling variant "Yamahide Shokuhin".

Latest inspection: Jul 5, 2019 · VAI

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

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Yamahide Shokuhin, Inc. FDA Warning Letters

1 warning letter on Dec 30, 2014.

Issued	Subject	Issuing office	Close-out letter
Dec 30, 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

2 inspections from Mar 28, 2014 to Jul 5, 2019.

Date	Site	Product	Classification	FEI
Jul 5, 2019	Miki, Japan	Food/Cosmetics	Voluntary Action Indicated (VAI)	3004249056
Mar 28, 2014	Miki, Japan	Food/Cosmetics	Official Action Indicated (OAI)	3004249056

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 Yamahide Shokuhin, Inc.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Dec 30, 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 3004249056	Miki, Japan	2	Jul 5, 2019

Yamahide Shokuhin, Inc. and the FDA: common questions

Has Yamahide Shokuhin, Inc. received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Yamahide Shokuhin, Inc.. The most recent is dated Dec 30, 2014.

Has Yamahide Shokuhin, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Yamahide Shokuhin, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Yamahide Shokuhin, Inc.?

The most recent FDA inspection on file ended Jul 5, 2019 at Miki, Japan and was classified VAI. FDA has 2 inspections of Yamahide Shokuhin, Inc. on file, 1 of them classified OAI (official action indicated).

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