483
CSL Plasma Inc.CSL Plasma Inc. – FDA 483, Dec 6, 2019
Record Details
An FDA inspection of CSL Plasma in Decatur, IL, from December 3-6, 2019, identified one observation. The firm was cited for failing to properly prepare a phlebotomy site, which resulted in contamination during a donor's venipuncture. This indicates a lapse in ensuring sterile conditions for blood collection.
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- Chicago District Office
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ID · 53740ca2-e34c-4308-b9ac-e341cd3ce210
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