FDA Inspection 764108 — Nexus CMF, LLC

Nexus CMF, LLC — FEI 3009702671

The FDA completed an inspection of Nexus CMF, LLC on January 20, 2012 in Cottonwood Heights, UT. 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
January 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cottonwood Heights, UT (United States)