# FDA Inspection 1167707 - OMNIlife Science, Inc. - March 11, 2022

Source: https://www.keypedia.com/records/fda_inspections/omnilife-science-inc/c700947e-fc90-406d-b477-e27a872f7495
Source feed: FDA_Inspections

> FDA Inspection 1167707 for OMNIlife Science, Inc. on March 11, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1167707
- Company Name: OMNIlife Science, Inc.
- Inspection Date: 2022-03-11
- 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 1167707 - 2022-03-11](https://www.keypedia.com/records/fda_inspections/omnilife-science-inc/724431a6-c354-44fd-b229-84a6a9ab1829)

Company: https://www.keypedia.com/companies/omnilife-science-inc/af642bb5-7613-4446-a3bf-37ce82bd91eb

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