FDA Inspection 554835 — Xodus Medical Inc

Xodus Medical Inc — FEI 1000221205

The FDA completed an inspection of Xodus Medical Inc on January 16, 2009 in New Kensington, PA. 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
January 16, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New Kensington, PA (United States)