FDA Inspection 680386 — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The FDA completed an inspection of PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. on Sep 21, 2010 in Best. 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
- Sep 21, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Best (Netherlands)