FDA Inspection 933942 — Philips Medical Systems DMC GmbH
The FDA completed an inspection of Philips Medical Systems DMC GmbH on Jul 9, 2015 in Hamburg. 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
- Jul 9, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Hamburg (Germany)