FDA Inspection 1119259 — Kenneth B. Strenge, MD
The FDA completed an inspection of Kenneth B. Strenge, MD on February 21, 2020 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
- February 21, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Paducah, KY (United States)
Additional Details
Clinical Investigator (CI)