FDA Inspection 970807 — Opocrin SPA

Opocrin SPA — FEI 3002807810

The FDA completed an inspection of Opocrin SPA on May 6, 2016 in Formigine. 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 6, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Formigine (Italy)