FDA Inspection
Siemens Healthcare Diagnostics Products GmbHSiemens Healthcare Diagnostics Products GmbH – FDA Inspection, Mar 26, 2009
Record Details
This FDA Inspection record concerns Siemens Healthcare Diagnostics Products GmbH, with an inspection on March 26, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 26, 2009
- Product Type
- Devices
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ID · 9b0bc0be-8d33-4c92-a9a7-e95da5d963ad
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 573266
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.100(a)(1)Analysis of data sources
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.184DHR content
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Other FDA inspections of Siemens Healthcare Diagnostics Products GmbH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 24, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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