FDA Inspection 1018937 — Guido Fanelli, M.D.

Guido Fanelli, M.D. — FEI 3013300859

The FDA completed an inspection of Guido Fanelli, M.D. on May 12, 2017 in Parma. 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
May 12, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Parma (Italy)

Additional Details

Clinical Investigator (CI)