FDA Inspection 583077 — Gambro Dialysatoren GmbH
The FDA completed an inspection of Gambro Dialysatoren GmbH on May 7, 2009 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
- May 7, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Hechingen (Germany)