FDA Inspection 809681 — Warner Chilcott Deutschland GmbH

Warner Chilcott Deutschland GmbH — FEI 3002808032

The FDA completed an inspection of Warner Chilcott Deutschland GmbH on November 8, 2012 in Weiterstadt. 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 8, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weiterstadt (Germany)