FDA Inspection 817926 — ERBE Elektromedizin GmbH
The FDA completed an inspection of ERBE Elektromedizin GmbH on Jan 31, 2013 in Tubingen. 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
- Jan 31, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Tubingen (Germany)