FDA Inspection 1005492 — Median Technologies
The FDA completed an inspection of Median Technologies on Jan 12, 2017 in Valbonne. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 12, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Valbonne (France)
Additional details
Sponsor, Contract Research Organization