Cylex, Inc.

Form 483

Columbia, Maryland, United StatesFEI 3003920771Issued December 17, 2008

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 3003920771.

Observations6

Issue DateDecember 17, 2008

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Cylex, Inc.
Location: Columbia, Maryland, United States
FEI Number: 3003920771
Product Type: Devices
Issue Date: December 17, 2008
Country: United States

Inspection History, 2008 to 2012

NAI1

VAI1

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

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Cylex, Inc. FDA Form 483, Columbia, Maryland, December 17, 2008