FDA Inspection 634572 — MED-EL Elektromedizinische Gereate, Gmbh
The FDA completed an inspection of MED-EL Elektromedizinische Gereate, Gmbh on Nov 26, 2009 in Innsbruck. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 26, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Innsbruck (Austria)