# FDA Inspection 1134650 - Batelle Corporate Operations IRB - December 08, 2020

Source: https://www.keypedia.com/records/fda_inspections/batelle-corporate-operations-irb/52fe97ae-a62b-4798-95fa-9930dfbd62ae
Source feed: FDA_Inspections

> FDA Inspection 1134650 for Batelle Corporate Operations IRB on December 08, 2020. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1134650
- Company Name: Batelle Corporate Operations IRB
- Inspection Date: 2020-12-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1134650 - 2020-12-08](https://www.keypedia.com/records/fda_inspections/batelle-corporate-operations-irb/4c8ba58a-2543-44e6-a135-d159ffc7538b)
- [FDA Inspection 1122516 - 2020-02-28](https://www.keypedia.com/records/fda_inspections/batelle-corporate-operations-irb/3c6d661d-16da-4ca0-963a-456d0ee7153b)
- [FDA Inspection 1122516 - 2020-02-28](https://www.keypedia.com/records/fda_inspections/batelle-corporate-operations-irb/ab8eee6f-6d68-47d7-a8b8-0f51e5e1dec7)
- [FDA Inspection 652158 - 2010-03-18](https://www.keypedia.com/records/fda_inspections/batelle-corporate-operations-irb/1ae31ab9-7501-4887-a030-6b4673128579)

Company: https://www.keypedia.com/companies/batelle-corporate-operations-irb/2d635497-d73e-49c5-ab05-4fe130deae56

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