FDA Inspection 1026433 — Dornier Medtech Laser GmbH
The FDA completed an inspection of Dornier Medtech Laser GmbH on Jul 20, 2017 in Wesling. 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 20, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wesling (Germany)