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KISCO US, INC — FDA Facility Profile

FEI 3030410117

KISCO US, INC is an FDA-inspected facility (FEI 3030410117) located in Fullerton, CA, US. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
May 13, 2026: Voluntary Action Indicated (VAI)
Inspections on record
1 (1 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

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 13, 2026Voluntary Action Indicated (VAI)Verification activity frequency (21 CFR 1.506(d)(1)(i))
Verification activity - appropriate (21 CFR 1.506(d)(1)(ii))
Audit - food safety regulation, plan (21 CFR 1.506(e)(1)(i)(B))

Facility details

Company
KISCO US, INC
Location
Fullerton, CA (US)
Source
inspections

FDA data resources

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