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Home > Newsletters > The GMP Letter > AngioDynamics Lacked Approval On Device Feature, 483 States

The GMP Letter

August 2012

AngioDynamics Lacked Approval On Device Feature, 483 States

A Form 483 for AngioDynamics of Queensbury, N.Y., states the company distributed a range of devices with flaws or unapproved features.

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