FDA-Inspected Site

Kevin E. Miller, MD

1 FDA inspection is on record for Kevin E. Miller, MD in Wichita, United States.

483· Form 483 issued

Wichita, United States · Last updated August 15, 2026

Overview

  • 1 FDA inspection is on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2026-02-13.

At a glance

Inspections

1

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
9 Feb 2026 – 13 Feb 2026Medical Devices & Rad Health483View 483 →

Observations on record

Form 483 observations cited at this site, most recent first.

13 Feb 2026
21 CFR 812.100

Investigator non-compliance with agreement/plan/regulations

Cited by Theressa B Smith

13 Feb 2026
21 CFR 812.110(a)

Subject participation prior to study approval

Cited by Theressa B Smith

13 Feb 2026
21 CFR 812.140(a)(3)(ii)

Investigator records of relevant observations inadequate

Cited by Theressa B Smith

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 812.100Cited across public-safe Form 483 observations1x
21 CFR 812.110(a)Cited across public-safe Form 483 observations1x
21 CFR 812.140(a)(3)(ii)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Kevin E. Miller, MD's 1 Form 483

Recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat