483
Henke Sass Wolf Of America,IncFDA 483 - Henke Sass Wolf Of America,Inc - September 16, 2025
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An FDA inspection of Henke Sass Wolf Of America, Inc in Dudley, MA, conducted from September 10-16, 2025, identified one observation. The firm lacked established procedures for acceptance activities, specifically for salvaged medical device goods used in manufacturing. This indicates a potential deficiency in ensuring component quality and adherence to specifications.
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