FDA Inspection 922994 — Varex Imaging Corporation

Varex Imaging Corporation — FEI 1318879

The FDA completed an inspection of Varex Imaging Corporation on March 31, 2015 in Liverpool, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 31, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Liverpool, NY (United States)