FDA Inspection 804101 — Memometal Technologies
The FDA completed an inspection of Memometal Technologies on Sep 26, 2012 in Bruz. 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
- Sep 26, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Bruz (France)