FDA Inspection 733413 — Medinol Ltd.

Medinol Ltd. — FEI 3003084171

The FDA completed an inspection of Medinol Ltd. on Jun 9, 2011 in Tel Aviv. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 9, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tel Aviv (Israel)

Additional Details

Sponsor, Contract Research Organization