FDA Inspection
Philips North America LLCPhilips North America LLC – FDA Inspection, Mar 19, 2012
Record Details
This FDA Inspection record concerns Philips North America LLC, with an inspection on March 19, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Philips North America LLC
- Inspection Date
- March 19, 2012
- Product Type
- Devices
View Company Profile
ID · 34868662-d263-4ea9-9857-3cb3be59124f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 772990
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.40Sponsors" general responsibilities
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Philips North America LLC
12| Date | Classification | Office | Project area |
|---|---|---|---|
| November 21, 2025 | Not classified | Seattle District Office | Compliance: Medical Devices |
| November 6, 2024 | Not classified | Seattle District Office | Compliance: Medical Devices |
| November 3, 2023 | Not classified | Seattle District Office | |
| October 27, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 20, 2021 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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