# FDA Inspection 1147392 - Deborah Heart & Lung Center IRB - July 26, 2021

Source: https://www.globalkeysolutions.net/records/fda_inspections/deborah-heart-lung-center-irb/3017ee34-9dfa-4ba6-aa15-a332a34d81e7
Source feed: FDA_Inspections

> FDA Inspection 1147392 for Deborah Heart & Lung Center IRB on July 26, 2021. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1147392
- Company Name: Deborah Heart & Lung Center IRB
- Inspection Date: 2021-07-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1147392 - 2021-07-26](https://www.globalkeysolutions.net/records/fda_inspections/deborah-heart-lung-center-irb/d919f38a-e59f-4f6a-b337-ae99785b79e9)
- [FDA Inspection 965697 - 2016-03-30](https://www.globalkeysolutions.net/records/fda_inspections/deborah-heart-lung-center-irb/942ad94b-e4e7-4ef2-a095-ac0dac6d60a6)
- [FDA Inspection 746974 - 2011-10-07](https://www.globalkeysolutions.net/records/fda_inspections/deborah-heart-lung-center-irb/30820356-c400-41a0-a77b-43642b70f61a)

Company: https://www.globalkeysolutions.net/companies/deborah-heart-lung-center-irb/901fdeb9-2f37-4c03-8954-e8d736dce7c0

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