FDA Inspection
Siemens Healthineers Ltd.Siemens Healthineers Ltd. – FDA Inspection, Sep 17, 2012
Record Details
This FDA Inspection record concerns Siemens Healthineers Ltd., with an inspection on September 17, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Siemens Healthineers Ltd.
- Inspection Date
- September 17, 2012
- Product Type
- Devices
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ID · c2a9ad90-e796-4c41-8776-ba5e17686a1b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 802825
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of Siemens Healthineers Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 22, 2017 | Not classified | Office of Inspections and Investigations |
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