FDA Inspection
Verathon, Inc.Verathon, Inc. – FDA Inspection, Jul 10, 2009
Record Details
This FDA Inspection record concerns Verathon, Inc., with an inspection on July 10, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Verathon, Inc.
- Inspection Date
- July 10, 2009
- Product Type
- Devices
View Company Profile
ID · c99fefbc-69d5-4226-bf48-7c4b4089a358
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 597628
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Verathon, Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| February 8, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 2, 2017 | Not classified | Seattle District Office | |
| November 3, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 3, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 23, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Verathon, Inc.
- FDA Inspection 1080797 - 2019-02-08
- FDA Inspection 1005931 - 2017-03-02
- FDA Inspection 992622 - 2016-11-03
- FDA Inspection 936910 - 2015-08-03
- FDA Inspection 888178 - 2014-07-23
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