FDA Inspection 677234 — Gyrus Medical Ltd.
The FDA completed an inspection of Gyrus Medical Ltd. on Aug 5, 2010 in Cardiff. 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 5, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Cardiff (United Kingdom)