FDA Inspection 1078109 — Anthony A Killeen MD

Anthony A Killeen MD — FEI 3014855669

The FDA completed an inspection of Anthony A Killeen MD on January 8, 2019 in Minneapolis, MN. 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 8, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

Clinical Investigator (CI)