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FDA Inspection
•Bausch Health Americas, Inc.•September 1, 2016

Bausch Health Americas, Inc. – FDA Inspection, Sep 1, 2016

Record Details

This FDA Inspection record concerns Bausch Health Americas, Inc., with an inspection on September 1, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Bausch Health Americas, Inc.
Inspection Date
September 1, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 8e71f0b1-ffc1-4f13-b4dd-d2dc3a79fca4

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
984875
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Bausch Health Americas, Inc.

5
DateClassificationOfficeProject area
September 11, 2024NAICenter for Devices and Radiological HealthCompliance: Devices
February 2, 2018NAICenter for Devices and Radiological HealthBioresearch Monitoring
May 10, 2017NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 28, 2015OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 26, 2014OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Bausch Health Americas, Inc.
  • FDA Inspection 1243801 - 2024-09-11
  • FDA Inspection 1044842 - 2018-02-02
  • FDA Inspection 1013201 - 2017-05-10
  • FDA Inspection 930190 - 2015-07-28
  • FDA Inspection 884972 - 2014-06-26

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