FDA Inspection
Philips North America, LLCPhilips North America, LLC – FDA Inspection, Dec 12, 2013
Record Details
This FDA Inspection record concerns Philips North America, LLC, with an inspection on December 12, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Philips North America, LLC
- Inspection Date
- December 12, 2013
- Product Type
- Devices
View Company Profile
ID · c1d1a994-e3aa-49d0-af85-5b430baa3b38
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 860079
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Philips North America, LLC
8| Date | Classification | Office | Project area |
|---|---|---|---|
| January 16, 2025 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 23, 2019 | Not classified | New England District Office | |
| December 4, 2018 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 14, 2017 | Not classified | New England District Office | |
| June 18, 2015 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Philips North America, LLC
- FDA Inspection 1260630 - 2025-01-16
- FDA Inspection 1142575 - 2019-08-23
- FDA Inspection 1073570 - 2018-12-04
- FDA Inspection 1034836 - 2017-07-14
- FDA Inspection 932660 - 2015-06-18
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