# Saint Bernards Medical Center IRB - Inspection Records

Source: https://www.keypedia.com/companies/saint-bernards-medical-center-irb/35bf5962-a6d1-469b-a71d-4b96b9c4d0ab

> Inspection records and compliance data for Saint Bernards Medical Center IRB in Jonesboro, Arkansas. Access full analysis and detailed observations.

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## Details

- Name: Saint Bernards Medical Center IRB
- FEI Number: 3009803114
- City: Jonesboro
- State: Arkansas
- Country Name: United States
- Address Line 1: 225 E Washington Ave
- Zip Code: 72401

## Related Documents

- [483 - Saint Bernards Medical Center IRB - 2022-05-26](https://www.keypedia.com/records/483/saint-bernards-medical-center-irb/b6c9880f-1f5f-4ccd-8e9e-724cf820eeb4) — source: FDA, date: May 26, 2022
- [483 - Saint Bernards Medical Center IRB - 2022-05-26](https://www.keypedia.com/records/483/saint-bernards-medical-center-irb/859f57b3-c771-4294-9484-5b8471e4d54b) — source: FDA, date: May 26, 2022
- [FDA Inspection 1170942 - Saint Bernards Medical Center IRB - 2022-05-26](https://www.keypedia.com/records/fda_inspections/saint-bernards-medical-center-irb/e111de1c-e264-42e6-ba4c-cd27df2cacf6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2022
- [FDA Inspection 1170942 - Saint Bernards Medical Center IRB - 2022-05-26](https://www.keypedia.com/records/fda_inspections/saint-bernards-medical-center-irb/472d392d-1074-4c4d-99cd-7d42369a2b5a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2022
- [FDA Inspection 1170942 - Saint Bernards Medical Center IRB - 2022-05-26](https://www.keypedia.com/records/fda_inspections/saint-bernards-medical-center-irb/bc48cac4-1587-40ff-9b59-1822c39d9855) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2022
- [FDA Inspection 821199 - Saint Bernards Medical Center IRB - 2013-02-27](https://www.keypedia.com/records/fda_inspections/saint-bernards-medical-center-irb/1b0ae6cc-1cf5-4efa-9fce-41d17c301cda) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 27, 2013

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