# FDA Inspection 912782 - Minneapolis VA Health Care System IRB - February 05, 2015

Source: https://www.keypedia.com/records/fda_inspections/minneapolis-va-health-care-system-irb/02fb3f0e-74a8-49ca-ae90-52de09f1084b
Source feed: FDA_Inspections

> FDA Inspection 912782 for Minneapolis VA Health Care System IRB on February 05, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 912782
- Company Name: Minneapolis VA Health Care System IRB
- Inspection Date: 2015-02-05
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1154335 - 2021-09-22](https://www.keypedia.com/records/fda_inspections/minneapolis-va-health-care-system-irb/f70ecdb5-ea85-4312-80b5-c6a4976e3f40)
- [FDA Inspection 1154335 - 2021-09-22](https://www.keypedia.com/records/fda_inspections/minneapolis-va-health-care-system-irb/8225324e-b032-45a7-acac-3a5d7967eaa1)
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Company: https://www.keypedia.com/companies/minneapolis-va-health-care-system-irb/631a7599-e349-4d8b-aaf1-1735370cb980

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