FDA Inspection 933313 — EUROIMMUN Medizinische Labordiagnostika AG
The FDA completed an inspection of EUROIMMUN Medizinische Labordiagnostika AG on Jun 11, 2015 in Lubeck. 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 11, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lubeck (Germany)