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FDA Inspection
•Fresenius Kabi Deutschland GmbH•April 11, 2018

Fresenius Kabi Deutschland GmbH – FDA Inspection, Apr 11, 2018

Record Details

This FDA Inspection record concerns Fresenius Kabi Deutschland GmbH, with an inspection on April 11, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Fresenius Kabi Deutschland GmbH
Inspection Date
April 11, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Steven P Donald (Issuing Officer)
View Company Profile

ID · a511328c-d1e1-4fe6-9eac-399f6a3af0ed

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1050946
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Fresenius Kabi Deutschland GmbH

3
DateClassificationOfficeProject area
October 19, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 5, 2019Not classifiedOffice of Inspections and Investigations
September 26, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Fresenius Kabi Deutschland GmbH
  • FDA Inspection 1208229 - 2022-10-19
  • FDA Inspection 1103462 - 2019-09-05
  • FDA Inspection 900868 - 2014-09-26

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