FDA Inspection 673807 — KDL Medical Inc

KDL Medical Inc — FEI 3002406063

The FDA completed an inspection of KDL Medical Inc on Jul 30, 2010 in Richardson, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 30, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Richardson, TX (United States)