FDA Inspection 907300 — Vibracare Gmbh
The FDA completed an inspection of Vibracare Gmbh on December 18, 2014 in Bremen. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- December 18, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bremen (Germany)