# Allendale IRB – FDA Inspection, Feb 23, 2011

Source: https://www.keypedia.com/records/fda_inspections/allendale-irb/c563b4da-9702-43b8-83d0-14f10ff7994a
Source feed: FDA_Inspections

> FDA inspection 713978 of Allendale IRB, February 23, 2011. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 56 and 812. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 713978
- Company Name: Allendale IRB
- Inspection Date: 2011-02-23
- 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: 3

## Related Documents

- FDA Inspection 1122441 - 2020-03-19
- [FDA Inspection 946552 - 2015-09-24](https://www.keypedia.com/records/fda_inspections/allendale-irb/a01ef777-c4fd-4638-8bcd-e15e65a13a9a)

Company: https://www.keypedia.com/companies/allendale-irb/2a85fab3-818e-44ac-8d23-1749a2abb8f9

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