483
Welch Allyn IncWelch Allyn Inc – FDA 483, Aug 17, 2023
Record Details
Welch Allyn Inc, a medical device manufacturer in Skaneateles Falls, NY, received one observation during an FDA inspection. The observation cited inadequately established procedures for corrective and preventive actions (CAPA). Specifically, one CAPA related to a recall lacked adequate verification of effectiveness for all corrective actions taken.
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ID · 24124108-6533-4fbf-a92a-2245f3a3628d
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