Syntermed, Inc.

Form 483

Atlanta, Georgia, United StatesFEI 3003079232Issued November 30, 2012

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 3003079232.

Observations4

Issue DateNovember 30, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Syntermed, Inc.
Location: Atlanta, Georgia, United States
FEI Number: 3003079232
Product Type: Devices
Issue Date: November 30, 2012
Country: United States

Inspection History, 2010 to 2022

NAI3

VAI1

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

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Syntermed, Inc. FDA Form 483, Atlanta, Georgia, November 30, 2012