Company
United StatesZiosoft USA, Inc., Newark, CA – FDA Inspections
Inspection records and compliance data for Ziosoft USA, Inc. in Newark, California. 3 FDA inspections on record, last inspected April 28, 2016.
Company Profile
This profile covers Ziosoft USA, Inc. based in Newark, California, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 0
- NAI
- 3
- Form 483s
- 0
- Warning letters
- 0
First inspected November 18, 2010. Last inspected April 28, 2016.
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| April 28, 2016 | NAI | Medical Devices & Rad Health · Compliance: Devices | 978225 |
| May 15, 2013 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 833418 |
| November 18, 2010 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 698540 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Ziosoft USA, Inc.
FEI Number
3009394491
Address
39899 Balentine Dr Ste 116, Newark, California 94560, United States
Country
United States
ID: f37d616d-c594-4801-99db-ebef6949b314