FDA Inspection 1099362 — Steven E. Kempers, MD

Steven E. Kempers, MD — FEI 3008407366

The FDA completed an inspection of Steven E. Kempers, MD on July 24, 2019 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
July 24, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
New Brighton, MN (United States)

Additional Details

Clinical BA/BE