FDA Inspection 629445 — Memometal Technologies
The FDA completed an inspection of Memometal Technologies on Oct 1, 2009 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
- Oct 1, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bruz (France)