FDA Inspection 1115255 — Itamar Medical Ltd.

Itamar Medical Ltd. — FEI 3003616071

The FDA completed an inspection of Itamar Medical Ltd. on December 19, 2019 in Caesarea. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 19, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Caesarea (Israel)

Citations

IDCFRDescription
311721 CFR 820.70(i)Software validation for automated processes