FDA Inspection 1099089 — Michael J. Kelner, M.D.
The FDA completed an inspection of Michael J. Kelner, M.D. on June 27, 2019 in San Diego, CA. 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
- June 27, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- San Diego, CA (United States)
Additional Details
Clinical Investigator (CI)