# FDA Inspection 1233779 - Revian Inc. - March 22, 2024

Source: https://www.keypedia.com/records/fda_inspections/revian-inc/08e24309-3d98-474d-b4df-3e6329772747
Source feed: FDA_Inspections

> FDA Inspection 1233779 for Revian Inc. on March 22, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1233779
- Company Name: Revian Inc.
- Inspection Date: 2024-03-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1233779 - 2024-03-22](https://www.keypedia.com/records/fda_inspections/revian-inc/c6f661d5-0e56-43ad-b60b-45fdacf7e6a5)

Company: https://www.keypedia.com/companies/revian-inc/e0062ac3-2c1d-4dbf-9367-ac99eb9017de

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