FDA Inspection 886826 — The Metrix Company

The Metrix Company — FEI 1000117446

The FDA completed an inspection of The Metrix Company on July 9, 2014 in Dubuque, IA. 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
July 9, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Dubuque, IA (United States)