Dynarex Corporation

Form 483

Orangeburg, New York, United StatesFEI 2431014Issued March 02, 2017

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 2431014.

Observations3

Issue DateMarch 02, 2017

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Dynarex Corporation
Location: Orangeburg, New York, United States
FEI Number: 2431014
Product Type: Devices
Issue Date: March 02, 2017
Country: United States

Inspection History, 2009 to 2017

NAI1

VAI3

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

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Dynarex Corporation FDA Form 483, Orangeburg, New York, March 2, 2017