# OMNIlife Science, Inc. – FDA Inspection, Aug 6, 2026

Source: https://www.keypedia.com/records/fda_inspections/omnilife-science-inc/80cf009f-40f1-4003-b68f-5ec54d8672cf
Source feed: FDA_Inspections

> FDA inspection 1329750 of OMNIlife Science, Inc., August 06, 2026. Classification: Voluntary Action Indicated (VAI). 1 citation. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1329750
- Company Name: OMNIlife Science, Inc.
- Inspection Date: 2026-08-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: San Francisco District Office
- Citation Count: 1

## Related Documents

- [FDA Inspection 1167707 - 2022-03-11](https://www.keypedia.com/records/fda_inspections/omnilife-science-inc/c700947e-fc90-406d-b477-e27a872f7495)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/richard-e-evoy/31c4827c-e0dc-4ddf-b516-714209b2515d)

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

Office: https://www.keypedia.com/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df