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FDA Inspection 1044842 — Bausch Health Americas, Inc.

Bausch Health Americas, Inc. — FEI 3009443653

The FDA completed an inspection of Bausch Health Americas, Inc. on February 2, 2018 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
February 2, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Rochester, NY (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1243801 (NAI Wed Sep 11 2024 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