FDA Inspection 1238698 — Kenneth B. Strenge, MD

Kenneth B. Strenge, MD — FEI 3015908064

The FDA completed an inspection of Kenneth B. Strenge, MD on May 16, 2024 in Paducah, KY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 16, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Paducah, KY (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations