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Many Non-U.S. Firms Affected by U.S. FDA Import Alert 80-04 for Medical Glove Manufacturing Defects, According to FDAImports.com, LLC
Date:5/3/2010

even petition FDA to obtain removal from the alerts.” The Alert states that after a third violation, the FDA’s Center for Device and Radiological Health (CDRH) will likely require the firm to undergo an FDA inspection or audit, and will require extensive proof to be removed from the Import Alert.

Whether your firm is in violation of Level 1, 2 or 3, FDAImports.com, LLC can help you get off IA 80-04. If you have entries subject to detention for apparent violations, or are simply concerned about your firm’s regulatory compliance, let FDAImports.com, LLC show you ‘the way through.” FDAImports.com, LLC is a consulting firm that can help your company get off of an Import Alert, as well as provide guidance to avoid future violations. Save your firm from expensive and time consuming delays, like that which IA 80-04 can cause, by contacting FDAImports.com, LLC. Foreign and domestic manufacturers who are in one of the above mentioned situations, or who desire to avoid such expensive problems, should contact FDAImports.com, LLC for expert advice and support.

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Read the full story at http://www.prweb.com/releases/FDA_Import_Alert/Medical_Glove_Defects/prweb3957724.htm.


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Many Non-U.S. Firms Affected by U.S. FDA Import Alert 80-04 for Medical Glove Manufacturing Defects, According to FDAImports.com, LLC
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