# FDA Inspection 1024079 - Omnilife USA, Inc. - September 01, 2017

Source: https://www.keypedia.com/records/fda_inspections/omnilife-usa-inc/3c8d8d05-d3c1-4a22-9e38-1e6b6bbe09ba
Source feed: FDA_Inspections

> FDA inspection 1024079 of Omnilife USA, Inc., September 01, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 111. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024079
- Company Name: Omnilife USA, Inc.
- Inspection Date: 2017-09-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Food Composition, Standards, Labeling and Econ
- Product Type: Food/Cosmetics
- Center: Foods & Cosmetics
- Office Name: Center for Food Safety and Applied Nutrition
- Citation Count: 2

## Related Documents

- FDA Inspection 1307088 - 2026-03-09

Company: https://www.keypedia.com/companies/omnilife-usa-inc/f01945ee-b401-42be-a0fc-29b58f44b314

Office: https://www.keypedia.com/offices/center-for-food-safety-and-applied-nutrition/e04dc4e5-ee4f-4b0d-be8c-1139531ddab2