FDA Inspection 935247 — Hermann Medizintechnik
The FDA completed an inspection of Hermann Medizintechnik on Jun 17, 2015 in Fridingen An Der Donau. 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 17, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Fridingen An Der Donau (Germany)