FDA Inspection
Siemens Healthcare Diagnostics Products Ltd.Siemens Healthcare Diagnostics Products Ltd. – FDA Inspection, Feb 8, 2018
Record Details
This FDA Inspection record concerns Siemens Healthcare Diagnostics Products Ltd., with an inspection on February 8, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- February 8, 2018
- Product Type
- Medical Devices & Rad Health
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ID · 98ed8b23-ee11-4c67-b0f8-85198688dcf8
Inspection Facts
- Inspection number
- 1042413
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
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Other FDA inspections of Siemens Healthcare Diagnostics Products Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 26, 2026 | NAI | Postmarket Assurance: Devices | |
| July 1, 2010 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Siemens Healthcare Diagnostics Products Ltd.
- FDA Inspection 1309226 - 2026-02-26
- FDA Inspection 672636 - 2010-07-01
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