FDA Inspection 705187 — Amundson, Dr Glenn

Amundson, Dr Glenn — FEI 3008727856

The FDA completed an inspection of Amundson, Dr Glenn on January 7, 2011 in Overland Park, KS. 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 7, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Overland Park, KS (United States)

Additional Details

Clinical Investigator (CI)