FDA Inspection 932175 — Accuray Incorporated

Accuray Incorporated — FEI 3005738050

The FDA completed an inspection of Accuray Incorporated on Jun 12, 2015 in Sunnyvale, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Sunnyvale, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.