FDA Inspection 1259266 — Philips Medical Systems Nederland B.V.
The FDA completed an inspection of Philips Medical Systems Nederland B.V. on Jan 17, 2025 in Eindhoven. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Jan 17, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Eindhoven (Netherlands)