483
Octapharma Plasma, Inc.Octapharma Plasma, Inc. – FDA 483, May 14, 2026
Record Details
An FDA inspection of Octapharma Plasma Inc in Mesa, AZ, a source plasma donation center, identified one observation. The primary concern was that equipment used for storing and distributing blood and blood components was not properly observed, standardized, or calibrated. Specifically, a printer used for plasma unit distribution labels lacked an installation qualification to verify label accuracy.
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ID · bb085cad-60f7-41ca-bc9f-d3e4a5570e6e
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