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Kevin E. Miller, MD — FDA Facility Profile

FEI 3042247790

Kevin E. Miller, MD is an FDA-inspected facility (FEI 3042247790) located in Wichita, KS, US. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
Feb 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
Form 483 and inspection documents
1 in FDA's reading room

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
Feb 13, 2026Voluntary Action Indicated (VAI)Investigator non-compliance with agreement/plan/regulations (21 CFR 812.100)
Subject participation prior to study approval (21 CFR 812.110(a))
Investigator records of relevant observations inadequate (21 CFR 812.140(a)(3)(ii))

Form 483s and inspection documents

Facility details

Company
Kevin E. Miller, MD
Location
Wichita, KS (US)
Source
inspections

FDA data resources

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