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FDA Inspection 1100982 — Brenntag Great Lakes, LLC

Brenntag Great Lakes, LLC — FEI 2126821

The FDA completed an inspection of Brenntag Great Lakes, LLC on August 2, 2019 in Menomonee Falls, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 2, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Menomonee Falls, WI (United States)

Facility

Other inspections at this facility

  • 1206296 (OAI Fri May 05 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1014704 (NAI Mon Jun 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 898055 (VAI Wed Sep 10 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768926 (VAI Tue Feb 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 721083 (VAI Fri Apr 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources