FDA Inspection
Church & Dwight Manufacturing Co., Ltd.Church & Dwight Manufacturing Co., Ltd. – FDA Inspection, Aug 12, 2024
Record Details
This FDA Inspection record concerns Church & Dwight Manufacturing Co., Ltd., with an inspection on August 12, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ea59da44-b3bc-42ce-af8d-5256790b331c
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1239809
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Church & Dwight Manufacturing Co., Ltd.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| August 8, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 15, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 31, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 13, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 24, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Church & Dwight Manufacturing Co., Ltd.
- FDA Inspection 1216861 - 2023-08-08
- FDA Inspection 1175612 - 2022-07-15
- FDA Inspection 1030421 - 2017-10-31
- FDA Inspection 917608 - 2015-03-13
- FDA Inspection 796146 - 2012-08-24
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