FDA Inspection 996967 — Steven E. Kempers, MD

Steven E. Kempers, MD — FEI 3008407366

The FDA completed an inspection of Steven E. Kempers, MD on December 12, 2016 in New Brighton, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 12, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
New Brighton, MN (United States)

Additional Details

Clinical Investigator (CI)