FDA Inspection
The Procter & Gamble Co.The Procter & Gamble Co. – FDA Inspection, Nov 26, 2012
Record Details
This FDA Inspection record concerns The Procter & Gamble Co., with an inspection on November 26, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- The Procter & Gamble Co.
- Inspection Date
- November 26, 2012
- Product Type
- Devices
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ID · cd00e37e-5f3b-45f8-b97b-9465f9c15b01
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 814797
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
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Other FDA inspections of The Procter & Gamble Co.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 22, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 2, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 24, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for The Procter & Gamble Co.
- FDA Inspection 1020805 - 2017-06-22
- FDA Inspection 880491 - 2014-06-02
- FDA Inspection 582163 - 2009-04-24
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