FDA Inspection 857072 — Maquet Cardiopulmonary GmbH
The FDA completed an inspection of Maquet Cardiopulmonary GmbH on Aug 15, 2013 in Hechingen. 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
- Aug 15, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hechingen (Germany)