FDA Inspection 869788 — Cilag AG

Cilag AG — FEI 3002806695

The FDA completed an inspection of Cilag AG on February 18, 2014 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
February 18, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Schaffhausen (Switzerland)