FDA Inspection 879756 — Stephen N. Davis, MD

Stephen N. Davis, MD — FEI 3010756732

The FDA completed an inspection of Stephen N. Davis, MD on May 20, 2014 in Towson, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 20, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Towson, MD (United States)

Additional Details

Sponsor, Contract Research Organization