# Ziosoft USA, Inc. – FDA Inspection, Nov 18, 2010

Source: https://www.keypedia.com/records/fda_inspections/ziosoft-usa-inc/f8d0b2af-a66a-4504-a3ed-b540652ba8e5
Source feed: FDA_Inspections

> FDA inspection 698540 of Ziosoft USA, Inc., November 18, 2010. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 698540
- Company Name: Ziosoft USA, Inc.
- Inspection Date: 2010-11-18
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 978225 - 2016-04-28
- FDA Inspection 833418 - 2013-05-15

Company: https://www.keypedia.com/companies/ziosoft-usa-inc/f37d616d-c594-4801-99db-ebef6949b314

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7