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