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

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Record Details

This FDA Inspection record concerns Murata Vios Inc., with an inspection on April 25, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company: Murata Vios Inc.
Inspection Date: April 25, 2024
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · f50e63ba-7291-4945-a594-b216d582ab09

Violation Codes2

21 CFR 820.18421 CFR 820.40

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