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FDA Inspection
•Unilever Manufacturing (US), Inc.•July 14, 2025

Unilever Manufacturing (US), Inc. – FDA Inspection, Jul 14, 2025

Record Details

This FDA Inspection record concerns Unilever Manufacturing (US), Inc., with an inspection on July 14, 2025, issued by the Kansas City District Office, covering foods & cosmetics.

Company
Unilever Manufacturing (US), Inc.
Inspection Date
July 14, 2025
Product Type
Foods & Cosmetics
Office
Kansas City District Office
View Company Profile

ID · fde2e7d7-b244-4b96-9a90-4fe4fb2aadc4

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1263635
FDA center
Foods & Cosmetics
Project area
Foodborne Biological Hazards
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 117.135(a)(1)Allergen preventive controls - Implement

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Unilever Manufacturing (US), Inc.

7
DateClassificationOfficeProject area
August 2, 2018Not classifiedKansas City District Office
March 23, 2017VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
April 4, 2014VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
April 4, 2014VAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
August 4, 2011NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
View all 7 other inspections on the company page
Other documents for Unilever Manufacturing (US), Inc.
  • FDA Inspection 1062822 - 2018-08-02
  • FDA Inspection 1007416 - 2017-03-23
  • FDA Inspection 873921 - 2014-04-04
  • FDA Inspection 872776 - 2014-04-04
  • FDA Inspection 739131 - 2011-08-04

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