483
VertiFlex, Inc.FDA 483 - VertiFlex, Inc. - July 19, 2016
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Record Details
VertiFlex, Inc., a medical device manufacturer in San Clemente, CA, was inspected by the FDA. The inspection revealed that device history records were not adequately maintained, specifically noting incomplete rework forms lacking required evaluation information. This indicates a deficiency in the firm's documentation practices.
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ID · b71bafc4-841e-4813-8149-9e7a109cac31