Murata Vios Inc. – FDA Inspection, Apr 25, 2024

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
Person: Dawn M. Braswell (Investigator)

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ID · f50e63ba-7291-4945-a594-b216d582ab09

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number: 1237095
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices

FDA Citations

21 CFR 820.40Procedures not adequately established or maintained
21 CFR 820.184Lack of or inadequate DHR procedures

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FDA Inspection

Murata Vios Inc.April 25, 2024