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Home » RightEye Receives Form 483 for Lax Design Controls and Other Failings
RightEye Receives Form 483 for Lax Design Controls and Other Failings
Eye movement tracking technology developer RightEye got a Form 483 for lapses in its design controls, product handling and complaint procedures, among other deficiencies observed during a June 28 to July 8 FDA inspection of its Bethesda, Md., facility.