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FDA Inspection
•EonNutra, LLC•October 25, 2012

EonNutra, LLC – FDA Inspection, Oct 25, 2012

Record Details

This FDA Inspection record concerns EonNutra, LLC, with an inspection on October 25, 2012, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
EonNutra, LLC
Inspection Date
October 25, 2012
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 4d777005-5789-4cc4-9119-0c46bee003f6

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
804816
FDA center
Foods & Cosmetics
Project area
Foodborne Biological Hazards

FDA Citations

14
  1. 21 CFR 111.83(a)Reserve sample - collect, hold
  2. 21 CFR 111.75(a)(2)Appropriate tests, examinations; certificate of analysis
  3. 21 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
  4. 21 CFR 111.353Manufacturing operations - written procedures
  5. 21 CFR 111.103Written procedure quality control operations material review
  6. 21 CFR 111.70(b)(1)Specifications - component identity
  7. 21 CFR 111.70(b)(2)Specifications-component purity, strength, composition
  8. 21 CFR 111.453Written procedures - holding
  9. 21 CFR 111.70(e)Specifications - identity, purity, strength, composition
  10. 21 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier

Showing 10 of 14 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of EonNutra, LLC

3
DateClassificationOfficeProject area
February 5, 2016OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
June 23, 2015OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
June 10, 2013OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
Other documents for EonNutra, LLC
  • FDA Inspection 958594 - 2016-02-05
  • FDA Inspection 928203 - 2015-06-23
  • FDA Inspection 835934 - 2013-06-10

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