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FDA Inspection
•Church & Dwight Co., Inc.•December 10, 2014

Church & Dwight Co., Inc. – FDA Inspection, Dec 10, 2014

Record Details

This FDA Inspection record concerns Church & Dwight Co., Inc., with an inspection on December 10, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Church & Dwight Co., Inc.
Inspection Date
December 10, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 4875d393-9a28-44e8-b7e9-9d4a50baebc6

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
906482
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.110(a)Control procedures to monitor and validate performance
  2. 21 CFR 211.160(a)Following/documenting laboratory controls
  3. 21 CFR 211.25(c)Inadequate number of personnel

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Church & Dwight Co., Inc.

6
DateClassificationOfficeProject area
April 14, 2026NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
October 25, 2024VAINew Jersey District OfficeDrug Quality Assurance
May 23, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 15, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 20, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Church & Dwight Co., Inc.
  • FDA Inspection 1292794 - 2026-04-14
  • FDA Inspection 1251801 - 2024-10-25
  • FDA Inspection 1090490 - 2019-05-23
  • FDA Inspection 1025390 - 2017-08-15
  • FDA Inspection 791038 - 2012-07-20

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