FDA Inspection 754443 — Ophtapharm AG

Ophtapharm AG — FEI 3005531475

The FDA completed an inspection of Ophtapharm AG on November 9, 2011 in Winterthur. 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
November 9, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Winterthur (Switzerland)