FDA Inspection 721119 — Catalent Anagni SRL

Catalent Anagni SRL — FEI 3002806546

The FDA completed an inspection of Catalent Anagni SRL on March 15, 2011 in Anagni. 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
March 15, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Anagni (Italy)