# Church & Dwight Manufacturing Co., Ltd. – FDA Inspection, Oct 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/church-dwight-manufacturing-co-ltd/87175bdd-e1e9-4e0e-b4b2-0811c815e1c4
Source feed: FDA_Inspections

> FDA inspection 1030421 of Church & Dwight Manufacturing Co., Ltd., October 31, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030421
- Company Name: Church & Dwight Manufacturing Co., Ltd.
- Inspection Date: 2017-10-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1239809 - 2024-08-12](https://www.keypedia.com/records/fda_inspections/church-dwight-manufacturing-co-ltd/ea59da44-b3bc-42ce-af8d-5256790b331c)
- FDA Inspection 1216861 - 2023-08-08
- FDA Inspection 1175612 - 2022-07-15
- FDA Inspection 917608 - 2015-03-13
- FDA Inspection 796146 - 2012-08-24

## Related Officers

- [Tiki Dixon](https://www.keypedia.com/people/tiki-dixon/b3160a2c-ef16-4fa2-b9b9-4c3a0ed17c5b)

Company: https://www.keypedia.com/companies/church-dwight-manufacturing-co-ltd/7c8a3735-e2d8-40ac-8efa-3efd263dd57f

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7