483
LV Liberty VisionFDA 483 - LV Liberty Vision - April 26, 2022
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Record Details
LV Liberty Vision, a medical device manufacturer in Portsmouth, NH, was cited for three significant quality system deficiencies. The inspection revealed inadequate design validation for their iWand P and Y-90 Disc, ineffective corrective and preventive action procedures, and a lack of established statistical techniques for process and product control. These issues indicate a need for improved quality management practices.
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