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FDA Inspection
•American Bottling Co. - Keurig Dr Pepper•January 31, 2013

FDA Inspection 815992 - American Bottling Co. - Keurig Dr Pepper - January 31, 2013

Record Details

This FDA Inspection record concerns American Bottling Co. - Keurig Dr Pepper, with an inspection on January 31, 2013, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
American Bottling Co. - Keurig Dr Pepper
Inspection Date
January 31, 2013
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 0eea2722-66be-44f9-8c27-983b0aecb83f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
815992
FDA center
Foods & Cosmetics
Project area
Foodborne Biological Hazards

FDA Citations

1
  1. 21 CFR 120.12(a)Records required - not maintained

Full citation text and observation details available on the Dashboard.

Other FDA inspections of American Bottling Co. - Keurig Dr Pepper

6
DateClassificationOfficeProject area
April 28, 2026NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
September 10, 2019NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
July 12, 2016NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
March 13, 2012OAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
October 4, 2011VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
View all 6 other inspections on the company page
Other documents for American Bottling Co. - Keurig Dr Pepper
  • FDA Inspection 1285272 - 2026-04-28
  • FDA Inspection 1102036 - 2019-09-10
  • FDA Inspection 976899 - 2016-07-12
  • FDA Inspection 771899 - 2012-03-13
  • FDA Inspection 749408 - 2011-10-04

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