FDA Inspection 1013201 - Bausch Health Americas, Inc. - May 10, 2017

FDA Inspection 1013201 for Bausch Health Americas, Inc. on May 10, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1013201 for Bausch Health Americas, Inc. on May 10, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Bausch Health Americas, Inc.

Inspection Date

May 10, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8f3ff5f-a2cf-4896-8151-c8bcf5fa164e

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