FDA Inspection 806425 — Accuray Incorporated

Accuray Incorporated — FEI 3005738050

The FDA completed an inspection of Accuray Incorporated on July 3, 2012 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
July 3, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Sunnyvale, CA (United States)