FDA Inspection 597702 — Technolas Perfect Vision GmbH
The FDA completed an inspection of Technolas Perfect Vision GmbH on Jul 23, 2009 in Munich. 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
- Jul 23, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Munich (Germany)