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FDA Inspection
•Fresenius Kabi Austria GMBH•July 3, 2009

Fresenius Kabi Austria GMBH – FDA Inspection, Jul 3, 2009

Record Details

This FDA Inspection record concerns Fresenius Kabi Austria GMBH, with an inspection on July 3, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Fresenius Kabi Austria GMBH
Inspection Date
July 3, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · ee06a231-8510-4d3c-a615-06e2a24f58a5

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
611006
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Fresenius Kabi Austria GMBH

12
DateClassificationOfficeProject area
March 21, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 28, 2023Not classifiedOffice of Inspections and Investigations
October 13, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 30, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 19, 2018Not classifiedOffice of Inspections and Investigations
View all 12 other inspections on the company page
Other documents for Fresenius Kabi Austria GMBH
  • FDA Inspection 1251340 - 2024-03-21
  • FDA Inspection 1205334 - 2023-03-28
  • FDA Inspection 1207391 - 2022-10-13
  • FDA Inspection 1162216 - 2020-01-30
  • FDA Inspection 1052462 - 2018-04-19

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