FDA Inspection 1177104 — Visionsense, Ltd.

Visionsense, Ltd. — FEI 3003143838

The FDA completed an inspection of Visionsense, Ltd. on Aug 4, 2022 in Petakh Tikva. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 4, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Petakh Tikva (Israel)

Citations

IDCFRDescription
340921 CFR 820.200(d)Service reports