FDA Inspection 895487 — Ki Mobility Llc

Ki Mobility Llc — FEI 3005905321

The FDA completed an inspection of Ki Mobility Llc on September 12, 2014 in Stevens Point, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 12, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Stevens Point, WI (United States)

Citations

IDCFRDescription
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency
405921 CFR 820.22Quality Audits - defined intervals