FDA Inspection 1004998 — Mipharm S.p.A.

Mipharm S.p.A. — FEI 3002807647

The FDA completed an inspection of Mipharm S.p.A. on February 3, 2017 in Milan. 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
February 3, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Milan (Italy)