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 or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 15, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Schaffhausen (Switzerland)

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