FDA Inspection 930148 — Accuray Incorporated

Accuray Incorporated — FEI 1000123585

The FDA completed an inspection of Accuray Incorporated on June 12, 2015 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
June 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)