FDA Inspection 714966 — Itamar Medical Ltd.

Itamar Medical Ltd. — FEI 3003616071

The FDA completed an inspection of Itamar Medical Ltd. on Jan 13, 2011 in Caesarea. 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
Jan 13, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Caesarea (Israel)

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