FDA Inspection
Bausch Health Americas, Inc.Bausch Health Americas, Inc. – FDA Inspection, May 10, 2017
Record Details
This FDA Inspection record concerns Bausch Health Americas, Inc., with an inspection on May 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · fbee8e43-b153-416c-a485-00e487f10d91
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1013201
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Bausch Health Americas, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 11, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 2, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 1, 2016 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 28, 2015 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 26, 2014 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Bausch Health Americas, Inc.
- FDA Inspection 1243801 - 2024-09-11
- FDA Inspection 1044842 - 2018-02-02
- FDA Inspection 984875 - 2016-09-01
- FDA Inspection 930190 - 2015-07-28
- FDA Inspection 884972 - 2014-06-26
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