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FDA Inspection 1250019 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1317628

The FDA completed an inspection of Bausch & Lomb Incorporated on September 9, 2024 in Rochester, NY. 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
September 9, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Rochester, NY (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1282260 (NAI Wed Jul 30 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1110911 (VAI Mon Nov 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1042701 (NAI Fri Feb 23 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1007875 (VAI Fri Mar 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 799524 (VAI Thu Sep 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources