FDA Inspection
Verathon, Inc.Verathon, Inc. – FDA Inspection, Jun 4, 2010
Record Details
This FDA Inspection record concerns Verathon, Inc., with an inspection on June 4, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Verathon, Inc.
- Inspection Date
- June 4, 2010
- Product Type
- Devices
View Company Profile
ID · 2d249110-01c4-46a9-bba1-7d57b8efded7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 666993
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(b)Documentation
- 21 CFR 820.40(b)Change records, content
Full citation text and observation details available on the Dashboard.
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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