FDA Inspection 937165 — Church & Dwight Inc

Church & Dwight Inc — FEI 2280705

The FDA completed an inspection of Church & Dwight Inc on August 6, 2015 in Princeton, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 6, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Princeton, NJ (United States)