# Inova Institutional Review Board (IRB) – FDA Inspection, Oct 30, 2013

Source: https://www.keypedia.com/records/fda_inspections/inova-institutional-review-board-irb/570326a1-bf2a-4c22-8808-50fd17cc4744
Source feed: FDA_Inspections

> FDA inspection 900995 of Inova Institutional Review Board (IRB), October 30, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 56. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900995
- Company Name: Inova Institutional Review Board (IRB)
- Inspection Date: 2013-10-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1223654 - 2023-11-16
- [FDA Inspection 1075242 - 2018-12-21](https://www.keypedia.com/records/fda_inspections/inova-institutional-review-board-irb/f57d3806-235d-4866-b6ea-38ea0b55b42a)
- FDA Inspection 548268 - 2008-11-03

Company: https://www.keypedia.com/companies/inova-institutional-review-board-irb/155a837a-2362-4f25-bdcf-b44d994a18b2

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