# FDA Inspection 1211473 - Biorez, Inc - August 04, 2023

Source: https://www.keypedia.com/records/fda_inspections/biorez-inc/0ba9da99-e4a2-4963-a610-fe831e8f0484
Source feed: FDA_Inspections

> FDA Inspection 1211473 for Biorez, Inc on August 04, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1211473
- Company Name: Biorez, Inc
- Inspection Date: 2023-08-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1317704 - 2026-05-13](https://www.keypedia.com/records/fda_inspections/biorez-inc/a3d41c99-b844-4b16-8058-d0d9f520ad4d)
- [FDA Inspection 1211473 - 2023-08-04](https://www.keypedia.com/records/fda_inspections/biorez-inc/fedd5639-1cbc-42c9-8837-76d5c31cad64)

Company: https://www.keypedia.com/companies/biorez-inc/b3836b32-8e27-4cd7-a515-84ba4b0e3ac0

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