# FDA Inspection 1223560 - Avreo Inc - September 12, 2023

Source: https://www.keypedia.com/records/fda_inspections/avreo-inc/18db5125-7a59-4859-84be-3de929b7e5ad
Source feed: FDA_Inspections

> FDA Inspection 1223560 for Avreo Inc on September 12, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1223560
- Company Name: Avreo Inc
- Inspection Date: 2023-09-12
- 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 1223560 - 2023-09-12](https://www.keypedia.com/records/fda_inspections/avreo-inc/308dad2b-af8d-4285-bc37-47b3a41d4858)
- [FDA Inspection 932465 - 2015-05-06](https://www.keypedia.com/records/fda_inspections/avreo-inc/7b90d4c9-2219-44e1-a444-7a0ddc171e52)

Company: https://www.keypedia.com/companies/avreo-inc/83f6ea43-b871-49d2-a7b9-450b49bd60eb

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