FDA Inspection 739595 — Stereotaxis Inc

Stereotaxis Inc — FEI 3006796025

The FDA completed an inspection of Stereotaxis Inc on Aug 15, 2011 in Tempe, AZ. 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
Aug 15, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Tempe, AZ (United States)