FDA Inspection 1012076 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 3003434767

The FDA completed an inspection of Bausch & Lomb Incorporated on April 28, 2017 in Irvine, CA. 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
April 28, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Irvine, CA (United States)