FDA Inspection
Church & Dwight IncChurch & Dwight Inc – FDA Inspection, Feb 13, 2012
Record Details
This FDA Inspection record concerns Church & Dwight Inc, with an inspection on February 13, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Church & Dwight Inc
- Inspection Date
- February 13, 2012
- Product Type
- Devices
View Company Profile
ID · 92eec106-6d34-4016-be07-602dc95974d4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 762722
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
5- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
- 21 CFR 820.186QSR
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Other FDA inspections of Church & Dwight Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 14, 2020 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 6, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 17, 2011 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Church & Dwight Inc
- FDA Inspection 1135841 - 2020-08-14
- FDA Inspection 937165 - 2015-08-06
- FDA Inspection 709138 - 2011-02-17
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