FDA Inspection 980973 — Olon S.P.A.

Olon S.P.A. — FEI 3002716636

The FDA completed an inspection of Olon S.P.A. on May 20, 2016 in Rodano. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 20, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rodano (Italy)

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