FDA Inspection 800098 — Xodus Medical Inc

Xodus Medical Inc — FEI 1000221205

The FDA completed an inspection of Xodus Medical Inc on September 21, 2012 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
September 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New Kensington, PA (United States)