FDA Inspection 1016055 — Hinnerk Wulf, M.D.

Hinnerk Wulf, M.D. — FEI 3013433094

The FDA completed an inspection of Hinnerk Wulf, M.D. on June 16, 2017 in Marburg. 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
June 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Marburg (Germany)

Additional Details

Clinical Investigator (CI)