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FDA Inspection 1243801 — Bausch Health Americas, Inc.

Bausch Health Americas, Inc. — FEI 3009443653

The FDA completed an inspection of Bausch Health Americas, Inc. on September 11, 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 11, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Rochester, NY (United States)

Facility

Other inspections at this facility

  • 1044842 (NAI Fri Feb 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1013201 (NAI Wed May 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984875 (OAI Thu Sep 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 930190 (OAI Tue Jul 28 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 884972 (OAI Thu Jun 26 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources