FDA Inspection 1194137 — Dornier Medtech GmbH
The FDA completed an inspection of Dornier Medtech GmbH on Dec 14, 2022 in Wessling. 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
- Dec 14, 2022
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wessling (Germany)