# FDA Inspection 1018301 - The Miriam Hospital IRB - June 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/the-miriam-hospital-irb/17433b71-4484-4ebe-9581-30639dd85fd5
Source feed: FDA_Inspections

> FDA Inspection 1018301 for The Miriam Hospital IRB on June 30, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018301
- Company Name: The Miriam Hospital IRB
- Inspection Date: 2017-06-30
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 649256 - 2010-01-27](https://www.keypedia.com/records/fda_inspections/the-miriam-hospital-irb/2e38b351-f3bd-446e-80d9-881e29729c9d)

Company: https://www.keypedia.com/companies/the-miriam-hospital-irb/3a601ebe-0177-43f6-acde-bfbf2a61ba08

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