FDA Inspection 1259055 - Vitrolife Inc. - January 23, 2025

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Record Details

This FDA Inspection record concerns Vitrolife Inc., with an inspection on January 23, 2025, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vitrolife Inc.
Inspection Date: January 23, 2025
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c7e0698f-175d-4f00-a188-60ad0bf49431

Violation Codes1

21 CFR 820.198(b)

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