FDA Inspection 1016949 — Kraff, Colman R., M.D.

Kraff, Colman R., M.D. — FEI 3001860833

The FDA completed an inspection of Kraff, Colman R., M.D. on June 29, 2017 in Chicago, IL. 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
June 29, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Clinical Investigator (CI)