FDA Inspection 819201 — Maquet SAS
The FDA completed an inspection of Maquet SAS on Feb 7, 2013 in Orleans Cedex 2. 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 7, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Orleans Cedex 2 (France)