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FDA Inspection 1119333 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 3003434767

The FDA completed an inspection of Bausch & Lomb Incorporated on February 28, 2020 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
February 28, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Irvine, CA (United States)

Facility

Other inspections at this facility

  • 1012076 (VAI Fri Apr 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 921919 (NAI Thu Mar 12 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 890108 (VAI Fri Jul 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 846970 (VAI Fri Aug 23 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 758988 (NAI Mon Dec 19 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources