# Verathon, Inc., Bothell, WA – FDA Inspections

Source: https://www.keypedia.com/companies/verathon-inc/4d196041-a0b4-4451-8406-b573d9bca0d2

> Inspection records and compliance data for Verathon, Inc. in Bothell, Washington. 8 FDA inspections on record, last inspected February 08, 2019.

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## Details

- Name: Verathon, Inc.
- FEI Number: 3022472
- Address Line 1: 20001 N Creek Pkwy
- City: Bothell
- State: Washington
- Zip Code: 98011
- Country Name: United States
- Address: 20001 N Creek Pkwy, Bothell, Washington 98011, United States
- Country: United States

## Related Documents

- FDA Inspection 1080797 - Verathon, Inc. - 2019-02-08 — classification: No Action Indicated (NAI), source: FDA, date: February 8, 2019
- FDA Inspection 1080797 - Verathon, Inc. - 2019-02-08 — classification: No Action Indicated (NAI), source: FDA, date: February 8, 2019
- FDA Inspection 1005931 - Verathon, Inc. - 2017-03-02 — source: FDA, date: March 2, 2017
- FDA Inspection 992622 - Verathon, Inc. - 2016-11-03 — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2016
- FDA Inspection 992622 - Verathon, Inc. - 2016-11-03 — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2016
- FDA Inspection 936910 - Verathon, Inc. - 2015-08-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 3, 2015
- [FDA Inspection 936910 - Verathon, Inc. - 2015-08-03](https://www.keypedia.com/records/fda_inspections/verathon-inc/625ca8d9-f8d2-4474-a735-086122be49bf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 3, 2015
- [FDA Inspection 888178 - Verathon, Inc. - 2014-07-23](https://www.keypedia.com/records/fda_inspections/verathon-inc/f1a4f6ad-439d-4202-9a3d-d1d078776b9a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 23, 2014
- FDA Inspection 888178 - Verathon, Inc. - 2014-07-23 — classification: No Action Indicated (NAI), source: FDA, date: July 23, 2014
- FDA Inspection 817364 - Verathon, Inc. - 2013-02-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 7, 2013

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