FDA Inspection
Philips North America, LLCPhilips North America, LLC – FDA Inspection, Jul 14, 2017
Record Details
This FDA Inspection record concerns Philips North America, LLC, with an inspection on July 14, 2017, issued by the New England District Office, covering medical devices & rad health.
- Company
- Philips North America, LLC
- Inspection Date
- July 14, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 84f42137-d8a6-46e7-aa25-b65f9237ab3c
Inspection Facts
- Inspection number
- 1034836
- 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 |
| August 23, 2019 | Not classified | New England District Office | |
| December 4, 2018 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 1142575 - 2019-08-23
- FDA Inspection 1073570 - 2018-12-04
- FDA Inspection 932660 - 2015-06-18
- FDA Inspection 860079 - 2013-12-12
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.