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

Source: https://www.globalkeysolutions.net/records/fda_inspections/viatris-inc/c3d3e8fd-9d6c-4f73-a069-fd791615bece/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099590
- Company Name: Viatris Inc.
- Inspection Date: 2019-08-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/viatris-inc/e65d242e-4279-4e07-992f-5f241792c2cf

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7