# FDA Inspection 1174242 - Kelvi - May 10, 2022

Source: https://www.keypedia.com/records/fda_inspections/kelvi/3e7bba0f-b771-4325-bd7d-7fd871e99efa
Source feed: FDA_Inspections

> FDA Inspection 1174242 for Kelvi on May 10, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1174242
- Company Name: Kelvi
- Inspection Date: 2022-05-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1174242 - 2022-05-10](https://www.keypedia.com/records/fda_inspections/kelvi/75e92582-c0e4-4083-93aa-cc788436f3aa)

Company: https://www.keypedia.com/companies/kelvi/de817127-ad2c-4d3e-a5be-5937fda2e5d5

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