# FDA Inspection 992622 - Verathon, Inc. - November 03, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/verathon-inc/f7f17b90-2c7e-4d89-ba40-144a83487d2d/
Source feed: FDA_Inspections

> FDA Inspection 992622 for Verathon, Inc. on November 03, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992622
- Company Name: Verathon, Inc.
- Inspection Date: 2016-11-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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