FDA Inspection 1230548 — Philips Medizin Systeme Boeblingen Gmbh
The FDA completed an inspection of Philips Medizin Systeme Boeblingen Gmbh on Mar 7, 2024 in Boblingen. 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
- Mar 7, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Boblingen (Germany)