FDA Inspection
Church & Dwight Manufacturing Co., Ltd.Church & Dwight Manufacturing Co., Ltd. – FDA Inspection, Oct 31, 2017
Record Details
This FDA Inspection record concerns Church & Dwight Manufacturing Co., Ltd., with an inspection on October 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 87175bdd-e1e9-4e0e-b4b2-0811c815e1c4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1030421
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Church & Dwight Manufacturing Co., Ltd.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| August 12, 2024 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| 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 |
| 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 1239809 - 2024-08-12
- FDA Inspection 1216861 - 2023-08-08
- FDA Inspection 1175612 - 2022-07-15
- FDA Inspection 917608 - 2015-03-13
- FDA Inspection 796146 - 2012-08-24
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