Gynex Corporation

Form 483

Redmond, Washington, United StatesFEI 3001238683Issued May 27, 2016

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 3001238683.

Observations6

Issue DateMay 27, 2016

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Gynex Corporation
Location: Redmond, Washington, United States
FEI Number: 3001238683
Product Type: Devices
Issue Date: May 27, 2016
Country: United States

Inspection History, 2009 to 2020

NAI1

VAI6

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

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Gynex Corporation FDA Form 483, Redmond, Washington, May 27, 2016