FDA Inspection 1097883 — GETSCH+HILLER MEDIZINTECHNIK GmbH
The FDA completed an inspection of GETSCH+HILLER MEDIZINTECHNIK GmbH on Jun 6, 2019 in Tuttlingen. 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
- Jun 6, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tuttlingen (Germany)