FDA Inspection 1009250 — Curia Italy S.r.l

Curia Italy S.r.l — FEI 3002807919

The FDA completed an inspection of Curia Italy S.r.l on March 31, 2017 in Rozzano. 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
March 31, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rozzano (Italy)