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483
•Welch Allyn Inc•August 17, 2023

Welch 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.

Company
Welch Allyn Inc
Inspection date
August 17, 2023
Product type
device
Office
Division of Human and Animal Food Operations - East I
Person
  • Matthew D. Schnittker
View Company Profile

ID · 24124108-6533-4fbf-a92a-2245f3a3628d

Other documents for Welch Allyn Inc
  • 483 - 2026-01-09January 9, 2026

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