483
QED, Inc.FDA 483 - QED, Inc. - February 26, 2020
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Record Details
QED, Inc., a medical device manufacturer in Lexington, KY, was cited for significant deficiencies in its quality system during an FDA inspection. The firm failed to adequately establish procedures for receiving, reviewing, and evaluating complaints. Additionally, records of complaint investigations were found to be incomplete, lacking required information.
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