NAMSA

Form 483

Minneapolis, Minnesota, United StatesFEI 3004109681Issued February 04, 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 3004109681.

Observations1

Issue DateFebruary 04, 2013

Status1 Related Warning Letter

Related Inspections5

Establishment Details

Firm: NAMSA
Location: Minneapolis, Minnesota, United States
FEI Number: 3004109681
Product Type: Devices
Issue Date: February 04, 2013
Country: United States

Inspection History, 2010 to 2023

NAI2

VAI3

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

Act on This Form 483

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NAMSA FDA Form 483, Minneapolis, Minnesota, February 4, 2013