FDA Inspection 654286 — Genesis Automation

Genesis Automation — FEI 3008262378

The FDA completed an inspection of Genesis Automation on Mar 22, 2010 in St Charles, IL. 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
Mar 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
St Charles, IL (United States)