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FDA Inspection
•Omnilife Manufactura S.A. de C.V.•November 27, 2012

Omnilife Manufactura S.A. de C.V. – FDA Inspection, Nov 27, 2012

Record Details

This FDA Inspection record concerns Omnilife Manufactura S.A. de C.V., with an inspection on November 27, 2012, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Omnilife Manufactura S.A. de C.V.
Inspection Date
November 27, 2012
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 7d704431-c2d3-43e9-ba6c-f2109ba9e438

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
809078
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ

FDA Citations

2
  1. 21 CFR 111.210(h)(3)(ii)(B)Components; add, verify
  2. 21 CFR 111.77(a)Specifications not met - reject, quality control

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Omnilife Manufactura S.A. de C.V.

2
DateClassificationOfficeProject area
December 6, 2018VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 31, 2009OAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
Other documents for Omnilife Manufactura S.A. de C.V.
  • FDA Inspection 1073580 - 2018-12-06
  • FDA Inspection 614261 - 2009-08-31

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