FDA Inspection 979662 — Accuray Incorporated

Accuray Incorporated — FEI 3005738050

The FDA completed an inspection of Accuray Incorporated on August 9, 2016 in Sunnyvale, CA. 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
August 9, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Sunnyvale, CA (United States)