Company
ChinaSiemens Shenzhen Magnetic Resonance Ltd. - MR, Shenzhen, China – FDA Inspections
Inspection records and compliance data for Siemens Shenzhen Magnetic Resonance Ltd. - MR in Shenzhen. 4 FDA inspections on record, 1 Form 483, last inspected August 23, 2018.
Company Profile
This profile covers Siemens Shenzhen Magnetic Resonance Ltd. - MR based in Shenzhen, China.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 1
- NAI
- 1
- Unclassified
- 2
- Form 483s
- 1
- Warning letters
- 0
First inspected February 12, 2015. Last inspected August 23, 2018.
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| August 23, 2018 | Not classified | Medical Devices & Rad Health | 1132618 |
| April 20, 2018 | Not classified | Medical Devices & Rad Health | 1079019 |
| March 3, 2017 | NAI | Medical Devices & Rad Health · Radiation Control and Health Safety Act | 1010359 |
| February 12, 2015 | VAI | Medical Devices & Rad Health · Compliance: Devices | 924210 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Siemens Shenzhen Magnetic Resonance Ltd. - MR
FEI Number
3004754211
Address
Siemens Mri Center, # 32 Gaoxin C. Avenu, Hi-Tech Industrial Park, Shenzhen, China
Country
China
ID: ad7b4444-8a23-44e5-822b-46d3fb18f734