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•Octapharma Plasma, Inc.•May 14, 2026

FDA 483 - Octapharma Plasma, Inc. - May 14, 2026

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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.

Company
Octapharma Plasma, Inc.
Inspection Date
May 14, 2026
Product Type
Biologics
Office
Division of Pharmaceutical Quality Operations IV
Person
  • Garrad R. Poole
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ID · bb085cad-60f7-41ca-bc9f-d3e4a5570e6e

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