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483
•Kashiv BioSciences, LLC•November 21, 2022

Kashiv BioSciences, LLC – FDA 483, Nov 21, 2022

Record Details

Kashiv BioSciences, LLC, a biological drug substance and drug product manufacturer in Chicago, IL, was cited with eight observations during an FDA inspection. The inspection revealed significant deficiencies across multiple areas, including inadequate aseptic process simulations, insufficient investigations into batch failures, and deficiencies in visual inspection programs and employee training. Additionally, issues were noted with cleaning and sanitization, component testing, process validation, and the stability program for Theragrastim pre-filled syringes.

Company
Kashiv BioSciences, LLC
Inspection date
November 21, 2022
Product type
biologics
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Thuy T. Nguyen ( Investigator, Consumer Safety Officer)
  • Muna Algharibeh (Investigator)
  • Laurimer Kuilan-Torres
View Company Profile

ID · 9e501626-8791-4d36-bea1-8a5b44ee1714

Other documents for Kashiv BioSciences, LLC
  • 483 - 2024-06-14June 14, 2024
  • 483 - 2022-01-14January 14, 2022
  • 483 - 2019-03-12March 12, 2019
  • EIR - 2019-03-12March 12, 2019
  • 483 - 2018-01-22January 22, 2018

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