FDA Inspection 854364 — Maquet Cardiopulmonary Gmbh
The FDA completed an inspection of Maquet Cardiopulmonary Gmbh on Sep 26, 2013 in Rastatt. 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
- Sep 26, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Rastatt (Germany)