FDA Inspection 1004998 — Mipharm S.P.A.

Mipharm S.P.A. — FEI 3002807647

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

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