Atlas

Form 483

Kevin E. Miller, MD Form 483, 2026-02-13

FDA issued a Form 483 to Kevin E. Miller, MD on 2026-02-13 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Kevin E. Miller, MD · Wichita, United States · Issued February 13, 2026

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

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

Inspected site

KEKevin E. Miller, MDWichita, United States

Inspection team

TBTheressa B Smith

Cited regulations

CFR citations associated with this Form 483.

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 483 report

Get the verbatim text of all 3 observations

The full inspection record, as Atlas holds it, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere