FDA Inspection 1260630 — Philips DS North America LLC
The FDA completed an inspection of Philips DS North America LLC on Jan 16, 2025 in Gainesville, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 16, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Gainesville, FL (United States)