FDA Inspection 1032543 — Siemens Healthcare Diagnostics Inc
The FDA completed an inspection of Siemens Healthcare Diagnostics Inc on Nov 9, 2017 in Elkhart, IN. 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
- Nov 9, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Elkhart, IN (United States)