FDA Inspection 711442 — Manocher Lashgari, M.D.
The FDA completed an inspection of Manocher Lashgari, M.D. on Feb 28, 2011 in Hartford, CT. 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
- Feb 28, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Hartford, CT (United States)
Additional Details
Clinical Investigator (CI)