FDA Inspection 796146 - Church & Dwight Manufacturing Co., Ltd. - August 24, 2012

FDA Inspection 796146 for Church & Dwight Manufacturing Co., Ltd. on August 24, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 796146 for Church & Dwight Manufacturing Co., Ltd. on August 24, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Church & Dwight Manufacturing Co., Ltd.

Inspection Date

August 24, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9d01e9d-8523-4efa-931b-11ab54f96b26

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