FDA Inspection 739708 — Bausch & Lomb Ireland Limited

Bausch & Lomb Ireland Limited — FEI 3002806454

The FDA completed an inspection of Bausch & Lomb Ireland Limited on Jul 21, 2011 in Waterford. 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
Jul 21, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Waterford (Ireland)