FDA Inspection 811733 — Natus Europe GmbH
The FDA completed an inspection of Natus Europe GmbH on Nov 15, 2012 in Planegg. 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
- Nov 15, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Planegg (Germany)