# Church & Dwight Manufacturing Co., Ltd. – FDA Inspection, Aug 12, 2024

Source: https://www.keypedia.com/records/fda_inspections/church-dwight-manufacturing-co-ltd/ea59da44-b3bc-42ce-af8d-5256790b331c
Source feed: FDA_Inspections

> FDA inspection 1239809 of Church & Dwight Manufacturing Co., Ltd., August 12, 2024. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1239809
- Company Name: Church & Dwight Manufacturing Co., Ltd.
- Inspection Date: 2024-08-12
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1216861 - 2023-08-08
- FDA Inspection 1175612 - 2022-07-15
- [FDA Inspection 1030421 - 2017-10-31](https://www.keypedia.com/records/fda_inspections/church-dwight-manufacturing-co-ltd/87175bdd-e1e9-4e0e-b4b2-0811c815e1c4)
- FDA Inspection 917608 - 2015-03-13
- FDA Inspection 796146 - 2012-08-24

## Related Officers

- [Investigator](https://www.keypedia.com/people/heath-a-gerber/3c47dcdd-875c-4f3c-8165-839354a53d8b)

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