Artivion, Inc

Form 483

Kennesaw, Georgia, United StatesFEI 3001451326Issued May 23, 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 3001451326.

Observations10

Issue DateMay 23, 2013

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Artivion, Inc
Location: Kennesaw, Georgia, United States
FEI Number: 3001451326
Product Type: Devices
Issue Date: May 23, 2013
Country: United States

Inspection History, 2010 to 2026

NAI6

VAI2

OAI2

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

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Artivion, Inc FDA Form 483, Kennesaw, Georgia, May 23, 2013