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FDA Inspection
•Brenntag Great Lakes, LLC•August 2, 2019

Brenntag Great Lakes, LLC – FDA Inspection, Aug 2, 2019

Record Details

This FDA Inspection record concerns Brenntag Great Lakes, LLC, with an inspection on August 2, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Brenntag Great Lakes, LLC
Inspection Date
August 2, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Michele L. Glendenning (FDA Associated Person)
  • Vaishali J. Patel
View Company Profile

ID · 1ab3c4c8-1c6e-4d53-9ffa-2209d9da6d48

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1100982
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Brenntag Great Lakes, LLC

5
DateClassificationOfficeProject area
May 5, 2023OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 12, 2017NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
September 10, 2014VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
February 28, 2012VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
April 15, 2011OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Brenntag Great Lakes, LLC
  • FDA Inspection 1206296 - 2023-05-05
  • FDA Inspection 1014704 - 2017-06-12
  • FDA Inspection 898055 - 2014-09-10
  • FDA Inspection 768926 - 2012-02-28
  • FDA Inspection 721083 - 2011-04-15

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