FDA Inspection 1026433 — Dornier Medtech Laser GmbH
The FDA completed an inspection of Dornier Medtech Laser GmbH on July 20, 2017 in Wesling. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 20, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Wesling (Germany)