FDA Inspection 803880 — Siemens Healthineers Ltd.

Siemens Healthineers Ltd. — FEI 3005150580

The FDA completed an inspection of Siemens Healthineers Ltd. on Sep 21, 2012 in Seongnam. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Seongnam (Korea (the Republic of))

Citations

IDCFRDescription
54621 CFR 820.75(a)Lack of or inadequate process validation

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