FDA Inspection 1030135 — Varian Medical Systems, Inc.

Varian Medical Systems, Inc. — FEI 3000206172

The FDA completed an inspection of Varian Medical Systems, Inc. on September 1, 2017 in Charlottesville, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 1, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Charlottesville, VA (United States)