FDA Inspection 812471 — John Agaiby MD

John Agaiby MD — FEI 3013669011

The FDA completed an inspection of John Agaiby MD on March 26, 2013 in Kenosha, WI. 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
March 26, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Kenosha, WI (United States)

Additional Details

Clinical Investigator (CI)