FDA Inspection 979676 — Accuray Incorporated

Accuray Incorporated — FEI 1000123585

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
Compliance: Devices
Location
Sunnyvale, CA (United States)