FDA Inspection 735874 — Stereotaxis, Inc.

Stereotaxis, Inc. — FEI 3003778388

The FDA completed an inspection of Stereotaxis, Inc. on Jul 14, 2011 in Maple Grove, MN. 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
Jul 14, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Maple Grove, MN (United States)

Additional Details

Postmarket Audit Inspections