FDA Inspection
Siemens Shenzhen Magnetic Resonance Ltd. - MRSiemens Shenzhen Magnetic Resonance Ltd. - MR – FDA Inspection, Aug 23, 2018
Record Details
This FDA Inspection record concerns Siemens Shenzhen Magnetic Resonance Ltd. - MR, with an inspection on August 23, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- August 23, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 601dcaff-2c58-47bb-bd1c-d1cb65a5c1a7
Inspection Facts
- Inspection number
- 1132618
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Siemens Shenzhen Magnetic Resonance Ltd. - MR
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 20, 2018 | Not classified | Office of Inspections and Investigations | |
| March 3, 2017 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| February 12, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Siemens Shenzhen Magnetic Resonance Ltd. - MR
- FDA Inspection 1079019 - 2018-04-20
- FDA Inspection 1010359 - 2017-03-03
- FDA Inspection 924210 - 2015-02-12
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