# FDA Inspection 1171454 - Avita Medial Americas Llc - April 29, 2022

Source: https://www.keypedia.com/records/fda_inspections/avita-medial-americas-llc/290c82d5-501d-4ad6-b78d-cd1eebadabde
Source feed: FDA_Inspections

> FDA Inspection 1171454 for Avita Medial Americas Llc on April 29, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1171454
- Company Name: Avita Medial Americas Llc
- Inspection Date: 2022-04-29
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1171454 - 2022-04-29](https://www.keypedia.com/records/fda_inspections/avita-medial-americas-llc/bbe9f19f-3c6e-42fd-b4c7-2846c710b154)
- [FDA Inspection 1050610 - 2018-02-23](https://www.keypedia.com/records/fda_inspections/avita-medial-americas-llc/81931851-b565-40ec-a21b-efac8494c579)
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- [FDA Inspection 786874 - 2012-06-07](https://www.keypedia.com/records/fda_inspections/avita-medial-americas-llc/b391d515-5c3d-41e7-abe0-77524ef4014b)

Company: https://www.keypedia.com/companies/avita-medial-americas-llc/56084a6d-17e6-459d-84db-7ea89a5a38e7

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