Mizutamari Shokuhin Co., Ltd. FDA Record

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

Mizutamari Shokuhin Co., Ltd. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Mizutamari Shokuhin Co., Ltd." is on file.

What these totals cover: FDA records filed under the name "Mizutamari Shokuhin Co., Ltd." and its spelling variant "Mizutamari Shokuhin Co".

Latest inspection
May 16, 2017 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA inspections

1 inspection on May 16, 2017.

DateSiteProductClassificationFEI
May 16, 2017Minamisatsuma, JapanFood/CosmeticsVoluntary Action Indicated (VAI)3013267376
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.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3013267376Minamisatsuma, Japan1May 16, 2017

Mizutamari Shokuhin Co., Ltd. and the FDA: common questions

Has Mizutamari Shokuhin Co., Ltd. received an FDA warning letter?

No FDA warning letter addressed to the name "Mizutamari Shokuhin Co., Ltd." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Mizutamari Shokuhin Co., Ltd. received an FDA Form 483?

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

When did the FDA last inspect Mizutamari Shokuhin Co., Ltd.?

The most recent FDA inspection on file ended May 16, 2017 at Minamisatsuma, Japan and was classified VAI. FDA has 1 inspection of Mizutamari Shokuhin Co., Ltd. on file.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.