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Yamahide Shokuhin, Inc. FDA Inspection Record

FEI 3004249056 · Inspections, Form 483s, warning letters and import refusals

Yamahide Shokuhin, Inc. is an FDA-inspected facility (FEI 3004249056) located in Miki, JP. RegDataLab tracks 2 FDA inspections and 1 compliance action at this facility.

What FDA found at this site

Latest inspection
Jul 5, 2019: Voluntary Action Indicated (VAI)
Inspections on record
2 (1 OAI, 1 VAI)
Last OAI inspection
Mar 28, 2014
Warning letters
1 listed by FDA for this FEI, latest Dec 30, 2014
Import refusals
10 or more

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Jul 5, 2019Voluntary Action Indicated (VAI)Sanitation monitoring (21 CFR 123.11(b))
HACCP plan implementation (21 CFR 123.6(b))
Mar 28, 2014Official Action Indicated (OAI)Corrective action per regulation (21 CFR 123.7(c))
HACCP training or qualification (21 CFR 123.10)
Food safety hazards (21 CFR 123.6(c)(1))

FDA record score

2 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

3 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIJul 5, 20196 x 0.251.5
Warning letter on FDA's dashboard, which does not show close-outsDec 30, 201410 years or older, so it adds no points0
Inspection classified OAIMar 28, 201410 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Yamahide Shokuhin, Inc.
Location
Miki (JP)
Source
inspections

Compliance actions

Import refusals

FDA data resources

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