FDA Inspection 1067565 — Pausch Medical GmbH
The FDA completed an inspection of Pausch Medical GmbH on August 15, 2018 in Erlangen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- August 15, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Erlangen (Germany)