# Verathon, Inc. – FDA Inspection, Aug 3, 2015

Source: https://www.keypedia.com/records/fda_inspections/verathon-inc/625ca8d9-f8d2-4474-a735-086122be49bf
Source feed: FDA_Inspections

> FDA inspection 936910 of Verathon, Inc., August 03, 2015. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 936910
- Company Name: Verathon, Inc.
- Inspection Date: 2015-08-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 1080797 - 2019-02-08
- FDA Inspection 1005931 - 2017-03-02
- FDA Inspection 992622 - 2016-11-03
- [FDA Inspection 888178 - 2014-07-23](https://www.keypedia.com/records/fda_inspections/verathon-inc/f1a4f6ad-439d-4202-9a3d-d1d078776b9a)
- FDA Inspection 817364 - 2013-02-07

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

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