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

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 · dc242a42-f0eb-4f73-bd1b-11223ed2fa25

Violation Codes1

21 CFR 820.198(b)

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