FDA Inspection 1099590 - Viatris Inc. - August 15, 2019

FDA Inspection 1099590 for Viatris Inc. on August 15, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1099590 for Viatris Inc. on August 15, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Viatris Inc.

Inspection Date

August 15, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: c3d3e8fd-9d6c-4f73-a069-fd791615bece

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