FDA Inspection 723621 — LivaNova Deutschland GmbH
The FDA completed an inspection of LivaNova Deutschland GmbH on Apr 13, 2011 in Munich. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection details
- Classification
- Official Action Indicated (OAI)
- End Date
- Apr 13, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Munich (Germany)