# FDA Inspection 1155777 - Missouri Baptist Med Ctr IRB - October 08, 2021

Source: https://www.keypedia.com/records/fda_inspections/missouri-baptist-med-ctr-irb/17afe7f4-6f64-437a-a2ef-e64e450acf4e
Source feed: FDA_Inspections

> FDA Inspection 1155777 for Missouri Baptist Med Ctr IRB on October 08, 2021. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1155777
- Company Name: Missouri Baptist Med Ctr IRB
- Inspection Date: 2021-10-08
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1155777 - 2021-10-08](https://www.keypedia.com/records/fda_inspections/missouri-baptist-med-ctr-irb/611eb34c-304c-4176-ab75-5e4c817e7063)
- [FDA Inspection 912332 - 2015-01-29](https://www.keypedia.com/records/fda_inspections/missouri-baptist-med-ctr-irb/0a6f7cfb-e08a-422c-8d69-2f367133d639)
- [FDA Inspection 578825 - 2009-04-30](https://www.keypedia.com/records/fda_inspections/missouri-baptist-med-ctr-irb/4fb88a23-907a-4774-a5d4-cf7259450a20)

Company: https://www.keypedia.com/companies/missouri-baptist-med-ctr-irb/20b0b8ac-1915-4a35-98da-637206ec6450

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