FDA Inspection
Philips North AmericaPhilips North America – FDA Inspection, Apr 13, 2012
Record Details
This FDA Inspection record concerns Philips North America, with an inspection on April 13, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Philips North America
- Inspection Date
- April 13, 2012
- Product Type
- Devices
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ID · 30d66b08-2cf6-4bf5-9820-18c0c8f31609
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 777361
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.20(b)Lack of or inadequate organizational structure
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Other FDA inspections of Philips North America
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 13, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 3, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 18, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Philips North America
- FDA Inspection 1224855 - 2023-12-13
- FDA Inspection 1005211 - 2017-03-03
- FDA Inspection 607750 - 2009-07-18
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