Gleemex Inc.

Form 483

Hicksville, New York, United StatesFEI 3006493132Issued January 28, 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 3006493132.

Observations2

Issue DateJanuary 28, 2009

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Gleemex Inc.
Location: Hicksville, New York, United States
FEI Number: 3006493132
Product Type: Devices
Issue Date: January 28, 2009
Country: United States

Inspection History, 2009 to 2011

NAI1

VAI1

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

Act on This Form 483

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Gleemex Inc. FDA Form 483, Hicksville, New York, January 28, 2009