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483
•Fresenius Kabi Compounding, LLC•November 5, 2025

Fresenius Kabi Compounding, LLC – FDA 483, Nov 5, 2025

Record Details

Fresenius Kabi Compounding, LLC in Canton, MA, received a Form FDA 483 with seven observations during an inspection from October 9 to November 5, 2025. The inspection revealed significant deficiencies in quality control, aseptic processing, environmental monitoring, and facility maintenance, particularly concerning defective IV bag ports and procedures to prevent microbiological contamination. These issues indicate a lack of thorough investigation, inadequate adherence to sterile compounding procedures, and poor facility upkeep.

Company
Fresenius Kabi Compounding, LLC
Inspection date
November 5, 2025
Product type
drugs
Office
New England District Office
People
  • Jonathan G. Matrisciano (Program Division Director/District Director)
  • Daniel L. Zheng (M.S., Consumer Safety Officer at FDA)
  • Lori M. Newman (Deputy Director)
View Company Profile

ID · 5c09f691-6d1d-4edc-88f7-402a9557988e

Other documents for Fresenius Kabi Compounding, LLC
  • 483 - 2023-03-06March 6, 2023
  • 483 - 2018-12-04December 4, 2018

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