# FDA Inspection 1238162 - U.S. Food and Drug Administration (FDA) Institutional Review Board (IRB) - May 08, 2024

Source: https://www.keypedia.com/records/fda_inspections/us-food-and-drug-administration-fda-institutional-review-board-irb/758bd80f-68b2-4aae-b8dc-ccca205051f7
Source feed: FDA_Inspections

> FDA Inspection 1238162 for U.S. Food and Drug Administration (FDA) Institutional Review Board (IRB) on May 08, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1238162
- Company Name: U.S. Food and Drug Administration (FDA) Institutional Review Board (IRB)
- Inspection Date: 2024-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 596054 - 2009-06-30](https://www.keypedia.com/records/fda_inspections/us-food-and-drug-administration-fda-institutional-review-board-irb/1f551b87-3ca4-4619-b7e3-b54d494cf7e7)

Company: https://www.keypedia.com/companies/us-food-and-drug-administration-fda-institutional-review-board-irb/010e4b18-113a-4483-bbeb-405662f230ef

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