# FDA Inspection 1279531 - Activbody, Inc. - August 22, 2025

Source: https://www.keypedia.com/records/fda_inspections/activbody-inc/9cb8ecf2-75c3-4187-9bcc-46015fb2ebe4
Source feed: FDA_Inspections

> FDA Inspection 1279531 for Activbody, Inc. on August 22, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1279531
- Company Name: Activbody, Inc.
- Inspection Date: 2025-08-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1279531 - 2025-08-22](https://www.keypedia.com/records/fda_inspections/activbody-inc/d768ccce-abc8-4a20-9240-f5c025732473)
- [FDA Inspection 1279531 - 2025-08-22](https://www.keypedia.com/records/fda_inspections/activbody-inc/400b0af8-1bf9-4e26-bca1-f6d97d21c50a)
- [FDA Inspection 1279531 - 2025-08-22](https://www.keypedia.com/records/fda_inspections/activbody-inc/6d5017d2-ae2c-4fb1-8c34-adb1b3dd4c69)

Company: https://www.keypedia.com/companies/activbody-inc/df5db145-7e8b-4df3-8d9c-1d6fe638deb3

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