FDA Inspection 823958 — Flowonix Medical Inc

Flowonix Medical Inc — FEI 3010079947

The FDA completed an inspection of Flowonix Medical Inc on March 21, 2013 in Mansfield, MA. 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
March 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Mansfield, MA (United States)