FDA Inspection
Philips Electronics North America CorporationPhilips Electronics North America Corporation – FDA Inspection, Aug 31, 2017
Record Details
This FDA Inspection record concerns Philips Electronics North America Corporation, with an inspection on August 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 31, 2017
- Product Type
- Devices
View Company Profile
ID · d19a8b7e-1f44-4797-be5d-23749eb13383
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1023742
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Philips Electronics North America Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 30, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Philips Electronics North America Corporation
- FDA Inspection 806265 - 2012-10-30
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