FDA Inspection 962375 — John S. Zakaib, MD

John S. Zakaib, MD — FEI 3011954234

The FDA completed an inspection of John S. Zakaib, MD on Feb 19, 2016 in Minneapolis, MN. 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
Feb 19, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

Clinical Investigator (CI)