FDA Inspection 917608 — Church & Dwight Manufacturing Co., Ltd.

Church & Dwight Manufacturing Co., Ltd. — FEI 1122329

The FDA completed an inspection of Church & Dwight Manufacturing Co., Ltd. on March 13, 2015 in South Chesterfield, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 13, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
South Chesterfield, VA (United States)

Citations

IDCFRDescription
317221 CFR 820.198(c)Investigation of device failures
369621 CFR 820.100(b)Documentation