FDA Inspection 1177939 — GETSCH+HILLER MEDIZINTECHNIK GmbH
The FDA completed an inspection of GETSCH+HILLER MEDIZINTECHNIK GmbH on Jul 21, 2022 in Tuttlingen. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Jul 21, 2022
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tuttlingen (Germany)