FDA Inspection 1230548 — Philips Medizin Systeme Boeblingen Gmbh
The FDA completed an inspection of Philips Medizin Systeme Boeblingen Gmbh on March 7, 2024 in Boblingen. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- March 7, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Boblingen (Germany)