# OMNILIFE USA – FDA Inspection, Sep 6, 2022

Source: https://www.keypedia.com/records/fda_inspections/omnilife-usa/b59f562d-8884-4d2c-a6dc-511248bcb8d5
Source feed: FDA_Inspections

> FDA inspection 1178212 of OMNILIFE USA, September 06, 2022. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 1. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1178212
- Company Name: OMNILIFE USA
- Inspection Date: 2022-09-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Foodborne Biological Hazards
- Product Type: Food/Cosmetics
- Center: Foods & Cosmetics
- Office Name: Center for Food Safety and Applied Nutrition
- Citation Count: 1

## Related Documents

- [FDA Inspection 1123947 - 2020-06-09](https://www.keypedia.com/records/fda_inspections/omnilife-usa/882b0544-08fc-475f-97d1-e4e2a8c3c7c4)

Company: https://www.keypedia.com/companies/omnilife-usa/352ef3fe-c32b-4aaa-b5ed-cb00dcd5e9a7

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