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FDA Inspection 1107226 — Bausch & Lomb Inc

Bausch & Lomb Inc — FEI 1920664

The FDA completed an inspection of Bausch & Lomb Inc on October 8, 2019 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 8, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Saint Louis, MO (United States)

Facility

Other inspections at this facility

  • 978030 (NAI Fri Jun 10 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 826558 (NAI Fri Mar 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 784537 (NAI Fri Jun 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 782300 (VAI Thu May 17 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources