FDA Inspection 829603 — Bioness Inc

Bioness Inc — FEI 3004553866

The FDA completed an inspection of Bioness Inc on April 30, 2013 in Valencia, CA. 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
April 30, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Valencia, CA (United States)