FDA Inspection
Philips North America, LLCPhilips North America, LLC – FDA Inspection, Aug 23, 2019
Record Details
This FDA Inspection record concerns Philips North America, LLC, with an inspection on August 23, 2019, issued by the New England District Office, covering medical devices & rad health.
- Company
- Philips North America, LLC
- Inspection Date
- August 23, 2019
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 71c3650f-6f4c-4f19-a44d-f35f9438d300
Inspection Facts
- Inspection number
- 1142575
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
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 |
| 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 |
| December 12, 2013 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Philips North America, LLC
- FDA Inspection 1260630 - 2025-01-16
- FDA Inspection 1073570 - 2018-12-04
- FDA Inspection 1034836 - 2017-07-14
- FDA Inspection 932660 - 2015-06-18
- FDA Inspection 860079 - 2013-12-12
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