483
CSL Plasma IncFDA 483 - CSL Plasma Inc - April 29, 2026
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An FDA inspection of CSL Plasma Inc's plasmapheresis center in Milwaukee, WI, identified a significant issue regarding donor notification. The firm failed to properly inform a permanently deferred donor of all relevant test results, specifically omitting results from a subsequent collection and certain test results from both collections. This indicates a lapse in the firm's donor communication procedures.
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