# FDA Inspection 1237095 - Murata Vios Inc. - April 25, 2024

Source: https://www.keypedia.com/records/fda_inspections/murata-vios-inc/f50e63ba-7291-4945-a594-b216d582ab09
Source feed: FDA_Inspections

> FDA Inspection 1237095 for Murata Vios Inc. on April 25, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1237095
- Company Name: Murata Vios Inc.
- Inspection Date: 2024-04-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/murata-vios-inc/833fbf1c-4652-424a-ace7-0f9034988d0f

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