FDA Inspection 807070 — Nonin Medical, Inc

Nonin Medical, Inc — FEI 2183646

The FDA completed an inspection of Nonin Medical, Inc on Nov 15, 2012 in Plymouth, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 15, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Plymouth, MN (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures