FDA Inspection 677596 — Hunkeler, Dr John D

Hunkeler, Dr John D — FEI 1928495

The FDA completed an inspection of Hunkeler, Dr John D on Aug 16, 2010 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
Aug 16, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Kansas City, MO (United States)

Additional Details

Clinical Investigator (CI)