FDA Inspection 1123114 — Curia Italy S.r.l.

Curia Italy S.r.l. — FEI 1000330416

The FDA completed an inspection of Curia Italy S.r.l. on May 17, 2019 in Origgio. 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 17, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Origgio (Italy)

Additional Details

Mutual Recognition Agreement (MRA)