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FDA Inspection 1030371 — Xodus Medical Inc

Xodus Medical Inc — FEI 1000221205

The FDA completed an inspection of Xodus Medical Inc on October 10, 2017 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
October 10, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New Kensington, PA (United States)

Facility

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  • 933965 (NAI Fri Jul 10 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 819556 (VAI Tue Feb 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 800098 (NAI Fri Sep 21 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources