FDA Inspection 982365 — Kenneth J. Rosenthal, M.D.
The FDA completed an inspection of Kenneth J. Rosenthal, M.D. on Aug 11, 2016 in Great Neck, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 11, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Great Neck, NY (United States)
Additional Details
Clinical Investigator (CI)