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FDA Inspection
•Nutripack LLC•April 15, 2009

Nutripack LLC – FDA Inspection, Apr 15, 2009

Record Details

This FDA Inspection record concerns Nutripack LLC, with an inspection on April 15, 2009, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Nutripack LLC
Inspection Date
April 15, 2009
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 9136ffb8-490d-49c7-be69-6ad6791065db

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
579101
FDA center
Foods & Cosmetics
Project area
Foodborne Biological Hazards

FDA Citations

33
  1. 21 CFR 113.100(b)Review not timely
  2. 21 CFR 113.40(a)(9)Suitable material
  3. 21 CFR 113.100(f)Distribution record
  4. 21 CFR 113.40(a)(2)Present each retort, accurate
  5. 21 CFR 110.35(c)Lack of effective pest exclusion
  6. 21 CFR 113.100(b)Entry not timely
  7. 21 CFR 113.40(a)(4)Steam controller
  8. 21 CFR 113.89Evaluation by process authority
  9. 21 CFR 113.83Records of process establishment
  10. 21 CFR 113.60(c)Coding - no mark, permanently visible

Showing 10 of 33 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Nutripack LLC

11
DateClassificationOfficeProject area
August 18, 2021VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
November 15, 2017VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
February 14, 2017OAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
February 14, 2017VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
November 14, 2012VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
View all 11 other inspections on the company page
Other documents for Nutripack LLC
  • FDA Inspection 1149809 - 2021-08-18
  • FDA Inspection 1031597 - 2017-11-15
  • FDA Inspection 1007834 - 2017-02-14
  • FDA Inspection 1004975 - 2017-02-14
  • FDA Inspection 807103 - 2012-11-14

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