Home / Facilities / 3009934446

Otoki Corporation Daepoong Factory FDA Inspection Record

FEI 3009934446 · Inspections, Form 483s, warning letters and import refusals

Otoki Corporation Daepoong Factory is an FDA-inspected facility (FEI 3009934446) located in Umseong-gun. RegDataLab tracks 3 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Sep 18, 2017: Voluntary Action Indicated (VAI)
Inspections on record
3 (3 VAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Import refusals
9

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
Sep 18, 2017Voluntary Action Indicated (VAI)Initial temperature of container contents (21 CFR 113.87(c))
Process records - forms missing information (21 CFR 113.100(a))
Incomplete information (21 CFR 113.100(e))
Processing: conform to other systems (21 CFR 113.40(j))
and 2 more
May 13, 2016Voluntary Action Indicated (VAI)Critical factor - scheduled process (21 CFR 113.40(i))
HACCP plan location (21 CFR 123.6(b))
Signed and dated (21 CFR 123.6(d))
Food safety hazards (21 CFR 123.6(c)(1))
Jul 22, 2011Voluntary Action Indicated (VAI)Supervisors (21 CFR 113.10)
Critical factors not stated (21 CFR 113.83)
Running water at suitable temperature (21 CFR 110.37(e))
As source of contamination (21 CFR 110.37(b)(3))
and 6 more

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 15, 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 VAISep 18, 20176 x 0.251.5
Inspection classified VAIMay 13, 201610 years or older, so it adds no points0
Inspection classified VAIJul 22, 201110 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 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 15, 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 15, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 15, 2026Newest record Nov 5, 2026Current

Reviewing Otoki Corporation Daepoong Factory as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Otoki Corporation Daepoong Factory yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Facility details

Company
Otoki Corporation Daepoong Factory
Location
Umseong-gun
Source
inspections

Import refusals

FDA data resources

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