# FDA Inspection 1262942 - Anteris Technologies Ltd - February 20, 2025

Source: https://www.keypedia.com/records/fda_inspections/anteris-technologies-ltd/858a6ad7-3ae9-4b71-874e-e57bd72808ad
Source feed: FDA_Inspections

> FDA Inspection 1262942 for Anteris Technologies Ltd on February 20, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1262942
- Company Name: Anteris Technologies Ltd
- Inspection Date: 2025-02-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1262942 - 2025-02-20](https://www.keypedia.com/records/fda_inspections/anteris-technologies-ltd/b875e910-8286-4f3c-8048-bd1e25cc66fb)
- [FDA Inspection 1262942 - 2025-02-20](https://www.keypedia.com/records/fda_inspections/anteris-technologies-ltd/0785e6ef-e825-4b49-8170-23132085be11)
- [FDA Inspection 1262942 - 2025-02-20](https://www.keypedia.com/records/fda_inspections/anteris-technologies-ltd/05ef86cd-7e5b-4e23-97dd-395a7e103634)
- [FDA Inspection 1180328 - 2022-08-16](https://www.keypedia.com/records/fda_inspections/anteris-technologies-ltd/2fa97067-6854-4937-8607-0ffb1fd88a54)
- [FDA Inspection 1180328 - 2022-08-16](https://www.keypedia.com/records/fda_inspections/anteris-technologies-ltd/51334839-37fc-434a-a65d-313a4c639b38)

Company: https://www.keypedia.com/companies/anteris-technologies-ltd/e06d6339-387b-41ab-91a1-77fc56bdc783

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d