FDA Inspection 582790 — Cilag AG

Cilag AG — FEI 3002806695

The FDA completed an inspection of Cilag AG on May 15, 2009 in Schaffhausen. 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 15, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Schaffhausen (Switzerland)