FDA Inspection 873626 — Rivopharm S.A.

Rivopharm S.A. — FEI 3005884589

The FDA completed an inspection of Rivopharm S.A. on April 3, 2014 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
April 3, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Manno (Switzerland)