FDA Inspection 762722 — Church & Dwight Inc

Church & Dwight Inc — FEI 2280705

The FDA completed an inspection of Church & Dwight Inc on February 13, 2012 in Princeton, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 13, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Princeton, NJ (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1472021 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
313021 CFR 820.100(a)Lack of or inadequate procedures
317521 CFR 820.186QSR
73221 CFR 803.50(a)(2)Individual Report of Malfunction