FDA Inspection 1017184 — Intraop Medical Corporation

Intraop Medical Corporation — FEI 3001874253

The FDA completed an inspection of Intraop Medical Corporation on May 25, 2017 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
May 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)