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FDA Inspection
•Omnilife USA, Inc.•September 1, 2017

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

Record Details

This FDA Inspection record concerns Omnilife USA, Inc., with an inspection on September 1, 2017, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Omnilife USA, Inc.
Inspection Date
September 1, 2017
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 3c8d8d05-d3c1-4a22-9e38-1e6b6bbe09ba

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1024079
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ

FDA Citations

2
  1. 21 CFR 111.465(b)Retain reserve samples - 1 year, 2 years
  2. 21 CFR 111.105(a)Quality control - processes, specifications, written procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Omnilife USA, Inc.

1
DateClassificationOfficeProject area
March 9, 2026NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
Other documents for Omnilife USA, Inc.
  • FDA Inspection 1307088 - 2026-03-09

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