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483
•Berkshire Sterile Manufacturing, LLC•October 21, 2024

Berkshire Sterile Manufacturing, LLC – FDA 483, Oct 21, 2024

Record Details

An FDA inspection of Berkshire Sterile Manufacturing in Lee, MA, revealed significant deficiencies in their sterile drug product manufacturing operations. Observations included inadequate aseptic processing procedures, insufficient environmental monitoring, and a lack of proper investigation into quality events. These findings indicate a high risk of microbial contamination and compromised product quality for their sterile injectable drug products.

Company
Berkshire Sterile Manufacturing, LLC
Inspection date
October 21, 2024
Product type
drugs
Office
Office of Medical Device and Radiological Health Operations
People
  • Andrea Franco (Pharmaceutical Scientist)
  • Hamed Touré
View Company Profile

ID · 72c404f5-4b36-435f-b842-75cb8d607994

Other documents for Berkshire Sterile Manufacturing, LLC
  • 483 - 2026-03-05March 5, 2026
  • 483 - 2024-06-12June 12, 2024
  • 483 - 2023-08-25August 25, 2023
  • 483 - 2023-01-20January 20, 2023
  • 483 - 2022-05-23May 23, 2022

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