FDA Inspection 1193504 — Kenneth B. Strenge, MD

Kenneth B. Strenge, MD — FEI 3015908064

The FDA completed an inspection of Kenneth B. Strenge, MD on December 8, 2022 in Paducah, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 8, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Paducah, KY (United States)

Additional Details

Clinical Investigator (CI)