FDA Inspection 848933 — Oxus, Inc.

Oxus, Inc. — FEI 3008841036

The FDA completed an inspection of Oxus, Inc. on September 20, 2013 in Auburn Hills, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Auburn Hills, MI (United States)

Citations

IDCFRDescription
333121 CFR 820.181DMR - not or inadequately maintained