483
Stryker CorporationFDA 483 - Stryker Corporation - November 21, 2019
Record Details
Stryker Corporation, a medical device manufacturer in San Jose, CA, was inspected by the FDA from November 12-21, 2019. The inspection identified one observation related to the firm's complaint handling procedures. Specifically, the firm failed to establish adequate timeliness deadlines for complaint processing, resulting in several complaints not being processed in a timely manner.
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ID · abf6d93e-220c-466e-b1d7-f683b0026ec5