FDA Inspection 1041892 — Medinol Ltd.

Medinol Ltd. — FEI 3003182398

The FDA completed an inspection of Medinol Ltd. on Aug 24, 2017 in Jerusalem. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 24, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Jerusalem (Israel)

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