483
OneBlood, Inc.OneBlood, Inc. – FDA 483, Jan 9, 2026
Record Details
An FDA inspection of OneBlood, Inc. in Thomasville, GA, on January 9, 2026, revealed a significant concern regarding phlebotomy site preparation. The inspection found that phlebotomists failed to maintain the sterility of the venipuncture site by allowing non-sterile items to touch the disinfected area during whole blood collections. This practice raises concerns about the assurance of a sterile container of Whole Blood.
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ID · 2476101a-606d-423b-a45d-84ff946aed81
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