FDA Inspection 1287232 — Olon SPA

Olon SPA — FEI 3002807048

The FDA completed an inspection of Olon SPA on May 24, 2024 in Capua. 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 24, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Capua (Italy)

Additional Details

Mutual Recognition Agreement (MRA)