Church & Dwight Manufacturing Co., Ltd.

Form 483

South Chesterfield, Virginia, United StatesFEI 1122329Issued March 13, 2015

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1122329.

Observations2

Issue DateMarch 13, 2015

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Church & Dwight Manufacturing Co., Ltd.
Location: South Chesterfield, Virginia, United States
FEI Number: 1122329
Product Type: Devices
Issue Date: March 13, 2015
Country: United States

Inspection History, 2010 to 2024

NAI3

VAI4

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Church & Dwight Manufacturing Co., Ltd. FDA Form 483, South Chesterfield, Virginia, March 13, 2015