FDA Inspection 1264905 — Rivopharm S.A.

Rivopharm S.A. — FEI 3005884589

The FDA completed an inspection of Rivopharm S.A. on June 23, 2023 in Manno. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 23, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Manno (Switzerland)

Additional Details

Mutual Recognition Agreement (MRA)