# Biorez, Inc – FDA Inspection, Aug 4, 2023

Source: https://www.keypedia.com/records/fda_inspections/biorez-inc/fedd5639-1cbc-42c9-8837-76d5c31cad64
Source feed: FDA_Inspections

> FDA inspection 1211473 of Biorez, Inc, August 04, 2023. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1211473
- Company Name: Biorez, Inc
- Inspection Date: 2023-08-04
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1317704 - 2026-05-13

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jeffrey-j-thibodeau/62b74030-4aef-400b-8ae2-8bf84712d813)

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