FDA Inspection 672636 — Siemens Healthcare Diagnostics Products Ltd.
The FDA completed an inspection of Siemens Healthcare Diagnostics Products Ltd. on July 1, 2010 in Caernarfon. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 1, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Caernarfon (United Kingdom)
Additional Details
Postmarket Audit Inspections