FDA Inspection
Ziosoft USA, Inc.Ziosoft USA, Inc. – FDA Inspection, Nov 18, 2010
Record Details
This FDA Inspection record concerns Ziosoft USA, Inc., with an inspection on November 18, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Ziosoft USA, Inc.
- Inspection Date
- November 18, 2010
- Product Type
- Devices
View Company Profile
ID · f8d0b2af-a66a-4504-a3ed-b540652ba8e5
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 698540
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Ziosoft USA, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 28, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 15, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Ziosoft USA, Inc.
- FDA Inspection 978225 - 2016-04-28
- FDA Inspection 833418 - 2013-05-15
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