FDA Inspection 1053480 — 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 18, 2018 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 18, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Origgio (Italy)