FDA Inspection
Philips North America LLCPhilips North America LLC – FDA Inspection, Nov 21, 2025
Record Details
This FDA Inspection record concerns Philips North America LLC, with an inspection on November 21, 2025, issued by the Seattle District Office, covering medical devices & rad health.
- Company
- Philips North America LLC
- Inspection Date
- November 21, 2025
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · b25dfe5c-f2be-4b09-859f-625f96410493
Inspection Facts
- Inspection number
- 1292226
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Medical Devices
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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 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 |
| March 25, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Philips North America LLC
- FDA Inspection 1236344 - 2024-11-06
- FDA Inspection 1221815 - 2023-11-03
- FDA Inspection 1182153 - 2022-10-27
- FDA Inspection 1149323 - 2021-08-20
- FDA Inspection 1121760 - 2020-03-25
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