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FDA Inspection
•B Braun Melsungen Ag- Aktiengesellschaft•August 29, 2017

B Braun Melsungen Ag- Aktiengesellschaft – FDA Inspection, Aug 29, 2017

Record Details

This FDA Inspection record concerns B Braun Melsungen Ag- Aktiengesellschaft, with an inspection on August 29, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
B Braun Melsungen Ag- Aktiengesellschaft
Inspection Date
August 29, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Christophe T. Peters (Issuing Officer)
  • Kellia N. Hicks (FDA Associated Person)
View Company Profile

ID · edce242f-9d32-44a8-9913-4724ff5a2625

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1025753
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of B Braun Melsungen Ag- Aktiengesellschaft

3
DateClassificationOfficeProject area
November 13, 2024Not classifiedOffice of Inspections and Investigations
January 22, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 20, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for B Braun Melsungen Ag- Aktiengesellschaft
  • FDA Inspection 1263340 - 2024-11-13
  • FDA Inspection 1081920 - 2019-01-22
  • FDA Inspection 884341 - 2014-05-20

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