# FDA Inspection 1217721 - Baton Rouge General Medical Center IRB - September 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/baton-rouge-general-medical-center-irb/4de0c183-fd1a-4f9d-93f4-fb54d05cf6df
Source feed: FDA_Inspections

> FDA Inspection 1217721 for Baton Rouge General Medical Center IRB on September 14, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1217721
- Company Name: Baton Rouge General Medical Center IRB
- Inspection Date: 2023-09-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1217721 - 2023-09-14](https://www.keypedia.com/records/fda_inspections/baton-rouge-general-medical-center-irb/20efc76c-3435-4bab-b472-ca2e53751982)
- [FDA Inspection 1217721 - 2023-09-14](https://www.keypedia.com/records/fda_inspections/baton-rouge-general-medical-center-irb/a3d9f6b3-90e5-4b2f-825f-e81b0194e987)
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Company: https://www.keypedia.com/companies/baton-rouge-general-medical-center-irb/3939a926-623d-41d2-92bb-03615405ddef

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