FDA Inspection 733998 — Oridion Medical 1987 Ltd.

Oridion Medical 1987 Ltd. — FEI 3001227743

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.