Kevin E. Miller, MD – FDA Inspection, Feb 13, 2026

Record Details

This FDA Inspection record concerns Kevin E. Miller, MD, with an inspection on February 13, 2026, issued by the Kansas City District Office, covering medical devices & rad health.

Company: Kevin E. Miller, MD
Inspection Date: February 13, 2026
Product Type: Medical Devices & Rad Health
Office: Kansas City District Office
Person: Theressa B. Smith (Issuing Officer)

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ID · afb98266-54a5-4f28-8132-276f609c2a77

Inspection Facts

Inspection number: 1303334
FDA center: Medical Devices & Rad Health
Project area: Product Evaluation: Medical Devices
Outcome: Form 483 issued, view the record

FDA Citations

21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
21 CFR 812.110(a)Subject participation prior to study approval
21 CFR 812.140(a)(3)(ii)Investigator records of relevant observations inadequate

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FDA Inspection

Kevin E. Miller, MDFebruary 13, 2026