# FDA Inspection 1193918 - Integris Baptist Medical Center IRB - December 21, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/integris-baptist-medical-center-irb/1c16cbe1-9d04-4c7e-be77-ae17e093c0b6
Source feed: FDA_Inspections

> FDA Inspection 1193918 for Integris Baptist Medical Center IRB on December 21, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1193918
- Company Name: Integris Baptist Medical Center IRB
- Inspection Date: 2022-12-21
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1193918 - 2022-12-21](https://www.globalkeysolutions.net/records/fda_inspections/integris-baptist-medical-center-irb/dcd27e85-160e-4032-afbd-f5b413d7dabf)
- [FDA Inspection 1193918 - 2022-12-21](https://www.globalkeysolutions.net/records/fda_inspections/integris-baptist-medical-center-irb/0fb52b90-6e58-46e3-b12a-6b3f39ca47a0)
- [FDA Inspection 961043 - 2016-03-04](https://www.globalkeysolutions.net/records/fda_inspections/integris-baptist-medical-center-irb/ccf2ad92-ed9b-4d04-bc15-987efc9389a9)

Company: https://www.globalkeysolutions.net/companies/integris-baptist-medical-center-irb/2c6cc7f6-ad57-45fa-b482-fbc6b140c7e3

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