FDA Inspection 592784 — Siemens Healthineers Ltd.

Siemens Healthineers Ltd. — FEI 3002619337

The FDA completed an inspection of Siemens Healthineers Ltd. on May 21, 2009 in Seongnam. 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
May 21, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Seongnam (Korea (the Republic of))

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.