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American K.G.P., Inc FDA Inspection Record

FEI 3003133788 · Inspections, Form 483s, warning letters and import refusals

American K.G.P., Inc is an FDA-inspected facility (FEI 3003133788) located in Commerce, CA, US. RegDataLab tracks 3 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
May 2, 2025: Voluntary Action Indicated (VAI)
Inspections on record
3 (1 VAI, 2 NAI)
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

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
May 2, 2025Voluntary Action Indicated (VAI)Modified requirement: Temperature control - Implement (21 CFR 117.206(a))
Aug 7, 2018No Action Indicated (NAI)No citations listed
May 10, 2011No Action Indicated (NAI)No citations listed

Facility details

Company
American K.G.P., Inc
Location
Commerce, CA (US)
Source
inspections

FDA data resources

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