FDA Inspection 830380 — Nexus CMF, LLC

Nexus CMF, LLC — FEI 3009702671

The FDA completed an inspection of Nexus CMF, LLC on May 3, 2013 in Cottonwood Heights, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 3, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cottonwood Heights, UT (United States)

Citations

IDCFRDescription
343321 CFR 820.75(c)Process changes - review, evaluation and revalidation