FDA Inspection 1021856 — Gaetan Deslee, MD
The FDA completed an inspection of Gaetan Deslee, MD on July 6, 2017 in Reims Cedex. 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
- July 6, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Reims Cedex (France)
Additional Details
Clinical Investigator (CI)