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483
•Brenntag Great Lakes, LLC•May 5, 2023

Brenntag Great Lakes, LLC – FDA 483, May 5, 2023

Record Details

Brenntag Great Lakes, LLC, a manufacturer in Menomonee Falls, WI, was cited for significant quality control deficiencies during an FDA inspection. The firm failed to ensure proper review and approval of batch records and changes, did not conduct annual product reviews for several products, and exhibited issues with process validation for hand sanitizer manufacturing. Additionally, the inspection revealed unvalidated cleaning procedures for shared equipment and inadequate controls over computerized systems, including the use of a common login for a Gas Chromatography system.

Company
Brenntag Great Lakes, LLC
Inspection date
May 5, 2023
Product type
drugs
Office
Minneapolis District Office
Person
  • Nibin Varghese
View Company Profile

ID · 0f77baf6-9caf-4960-aeb7-c58ecd8822a1

Other documents for Brenntag Great Lakes, LLC
  • 483 - 2019-08-02August 2, 2019

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