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

Source: https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/dc242a42-f0eb-4f73-bd1b-11223ed2fa25
Source feed: FDA_Inspections

> FDA Inspection 1259055 for Vitrolife Inc. on January 23, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259055
- Company Name: Vitrolife Inc.
- Inspection Date: 2025-01-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1259055 - 2025-01-23](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/195a4df1-91ba-464a-b337-ae29cfbd243f)
- [FDA Inspection 1259055 - 2025-01-23](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/b041cd38-08ff-46e6-894f-086e1fb7f71a)
- [FDA Inspection 1259055 - 2025-01-23](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/c7e0698f-175d-4f00-a188-60ad0bf49431)
- [FDA Inspection 1149812 - 2021-08-19](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/862384ef-1a36-4262-890d-9424d1c2a7a3)
- [FDA Inspection 1149812 - 2021-08-19](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/08e3cb8d-911f-436d-91cd-abd62550c3ca)

Company: https://www.globalkeysolutions.net/companies/vitrolife-inc/386a7084-7769-4be3-9a8e-9495a5ca7615

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