FDA 483 - Symmetry Medical Manufacturing, Inc. - October 21, 2022

Symmetry Medical Manufacturing, Inc., a medical device manufacturer in Manchester, NH, was issued a Form FDA 483 following an inspection from October 13-21, 2022. The inspection revealed a significant deficiency in the firm's corrective and preventive action procedures, specifically regarding the failure to address systemic document control issues identified in multiple internal reports. This indicates a breakdown in the quality system's ability to manage and control essential documentation.