# FDA Inspection 1209486 - MetroHealth Medical Center IRB - June 22, 2023

Source: https://www.keypedia.com/records/fda_inspections/metrohealth-medical-center-irb/967e2ff8-caad-40e3-bb86-e844485181e7
Source feed: FDA_Inspections

> FDA Inspection 1209486 for MetroHealth Medical Center IRB on June 22, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1209486
- Company Name: MetroHealth Medical Center IRB
- Inspection Date: 2023-06-22
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1059184 - 2018-06-22](https://www.keypedia.com/records/fda_inspections/metrohealth-medical-center-irb/613a2bac-6ddf-44a8-b8e0-9aa847248aac)
- [FDA Inspection 844809 - 2013-08-13](https://www.keypedia.com/records/fda_inspections/metrohealth-medical-center-irb/74a28b69-dfef-49ac-b6fc-ec32cbfd68e4)
- [FDA Inspection 844809 - 2013-08-13](https://www.keypedia.com/records/fda_inspections/metrohealth-medical-center-irb/afdd3163-8d8b-40f0-813d-bd4bcbf505c9)

Company: https://www.keypedia.com/companies/metrohealth-medical-center-irb/dd2147f8-ae90-4369-919d-806bd3131491

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