FDA Inspection 733998 — Oridion Medical 1987 Ltd.
The FDA completed an inspection of Oridion Medical 1987 Ltd. on June 15, 2011 in Jerusalem. 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
- June 15, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Jerusalem (Israel)