FDA Inspection 719159 — Steinke, Kurt

Steinke, Kurt — FEI 3008851331

The FDA completed an inspection of Steinke, Kurt on Apr 4, 2011 in Chandler, AZ. 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
Apr 4, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Chandler, AZ (United States)

Additional Details

Clinical Investigator (CI)