FDA Inspection 776330 — Hovione Limited

Hovione Limited — FEI 3008058822

The FDA completed an inspection of Hovione Limited on Mar 16, 2012 in Ringaskiddy. 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
Mar 16, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ringaskiddy (Ireland)