Verathon, Inc.

Form 483

Bothell, Washington, United StatesFEI 3022472Issued February 07, 2013

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3022472.

Observations2

Issue DateFebruary 07, 2013

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Verathon, Inc.
Location: Bothell, Washington, United States
FEI Number: 3022472
Product Type: Devices
Issue Date: February 07, 2013
Country: United States

Inspection History, 2009 to 2019

NAI2

VAI5

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Verathon, Inc. FDA Form 483, Bothell, Washington, February 7, 2013