FDA Inspection 1063574 — Olon S.p.A.

Olon S.p.A. — FEI 3002716636

The FDA completed an inspection of Olon S.p.A. on March 3, 2017 in Rodano. 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 3, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rodano (Italy)

Additional Details

Mutual Recognition Agreement (MRA)