# FDA Inspection 1109738 - Asentral Inc. IRB - October 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/asentral-inc-irb/4ff10e9d-9506-4094-991e-4b4d1e20cce4
Source feed: FDA_Inspections

> FDA Inspection 1109738 for Asentral Inc. IRB on October 24, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1109738
- Company Name: Asentral Inc. IRB
- Inspection Date: 2019-10-24
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1109738 - 2019-10-24](https://www.keypedia.com/records/fda_inspections/asentral-inc-irb/a3976141-a070-4b0e-936a-bac17c1fb599)
- [FDA Inspection 832470 - 2013-05-14](https://www.keypedia.com/records/fda_inspections/asentral-inc-irb/ebb0501c-739e-4e1d-97c9-0cdff7f4166b)

Company: https://www.keypedia.com/companies/asentral-inc-irb/e0077815-ec88-468f-bbaf-54851eba43a0

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