FDA Inspection 843790 — Philips Medical Systems DMC GmbH
The FDA completed an inspection of Philips Medical Systems DMC GmbH on Jun 14, 2013 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
- Jun 14, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Hamburg (Germany)