Dornier Medtech America, Inc.

Form 483

Kennesaw, Georgia, United StatesFEI 1037955Issued March 05, 2010

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 1037955.

Observations3

Issue DateMarch 05, 2010

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Dornier Medtech America, Inc.
Location: Kennesaw, Georgia, United States
FEI Number: 1037955
Product Type: Devices
Issue Date: March 05, 2010
Country: United States

Inspection History, 2010 to 2017

NAI2

VAI1

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

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Dornier Medtech America, Inc. FDA Form 483, Kennesaw, Georgia, March 5, 2010