# FDA Inspection 1170741 - iHealth Labs, Inc. - May 16, 2022

Source: https://www.keypedia.com/records/fda_inspections/ihealth-labs-inc/e1b540b6-9c05-44c8-b352-82d26c3b72de
Source feed: FDA_Inspections

> FDA Inspection 1170741 for iHealth Labs, Inc. on May 16, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1170741
- Company Name: iHealth Labs, Inc.
- Inspection Date: 2022-05-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1231538 - 2024-05-08](https://www.keypedia.com/records/fda_inspections/ihealth-labs-inc/6420143e-9d60-4610-9cf8-058470d88efc)
- [FDA Inspection 1231538 - 2024-05-08](https://www.keypedia.com/records/fda_inspections/ihealth-labs-inc/32a007d3-1327-4212-b771-71e74dcd4bc5)

Company: https://www.keypedia.com/companies/ihealth-labs-inc/c321322d-cae3-4e8a-b7fc-8b5484fc3322

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