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FDA Inspection
•Fresenius Kabi (Brunna Facility) AB•September 23, 2016

Fresenius Kabi (Brunna Facility) AB – FDA Inspection, Sep 23, 2016

Record Details

This FDA Inspection record concerns Fresenius Kabi (Brunna Facility) AB, with an inspection on September 23, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Fresenius Kabi (Brunna Facility) AB
Inspection Date
September 23, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 31eeeb6a-b6c7-4310-bfa2-9d848854f9bf

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
992242
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Fresenius Kabi (Brunna Facility) AB

4
DateClassificationOfficeProject area
September 21, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 23, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 11, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 30, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Fresenius Kabi (Brunna Facility) AB
  • FDA Inspection 1273191 - 2023-09-21
  • FDA Inspection 1140314 - 2019-05-23
  • FDA Inspection 876535 - 2014-04-11
  • FDA Inspection 751067 - 2011-06-30

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