# FDA Inspection 995375 - IRB  Inc - November 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/irb-inc/06ab42a2-22ff-48e9-99db-1408ee160742
Source feed: FDA_Inspections

> FDA Inspection 995375 for IRB  Inc on November 29, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 995375
- Company Name: IRB  Inc
- Inspection Date: 2016-11-29
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 643205 - 2010-02-04](https://www.keypedia.com/records/fda_inspections/irb-inc/10ac36a6-f14b-4d23-8d46-0f507d40371b)

Company: https://www.keypedia.com/companies/irb-inc/0d4c86ce-480f-46e6-be33-5edbb1c0bd7c

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