FDA Inspection 714996 — Harper, Dr Diane M

Harper, Dr Diane M — FEI 3008730305

The FDA completed an inspection of Harper, Dr Diane M on Mar 3, 2011 in Kansas City, MO. 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 3, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Kansas City, MO (United States)

Additional Details

Clinical Investigator (CI)