Atritech, Inc

Form 483

Plymouth, Minnesota, United StatesFEI 3007338617Issued February 04, 2009

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 3007338617.

Observations3

Issue DateFebruary 04, 2009

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Atritech, Inc
Location: Plymouth, Minnesota, United States
FEI Number: 3007338617
Product Type: Devices
Issue Date: February 04, 2009
Country: United States

Inspection History, 2009

NAI1

VAI1

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

Act on This Form 483

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Atritech, Inc FDA Form 483, Plymouth, Minnesota, February 4, 2009