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FDA Inspection 1090490 — Church & Dwight Co., Inc.

Church & Dwight Co., Inc. — FEI 2224549

The FDA completed an inspection of Church & Dwight Co., Inc. on May 23, 2019 in Lakewood, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 23, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lakewood, NJ (United States)

Facility

Other inspections at this facility

  • 1292794 (NAI Tue Apr 14 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1251801 (VAI Fri Oct 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025390 (NAI Tue Aug 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 906482 (VAI Wed Dec 10 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791038 (NAI Fri Jul 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources