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FDA Inspection
•Fresenius Kabi Austria Gmbh•March 24, 2017

Fresenius Kabi Austria Gmbh – FDA Inspection, Mar 24, 2017

Record Details

This FDA Inspection record concerns Fresenius Kabi Austria Gmbh, with an inspection on March 24, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Fresenius Kabi Austria Gmbh
Inspection Date
March 24, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Massoud Motamed (FDA Associated Person)
View Company Profile

ID · 5de8cbe2-2f09-4d2d-9e06-6ffd76d8f8d1

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1006761
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Fresenius Kabi Austria Gmbh

5
DateClassificationOfficeProject area
May 23, 2025Not classifiedOffice of Inspections and Investigations
July 15, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 27, 2018Not classifiedOffice of Inspections and Investigations
November 7, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 29, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Fresenius Kabi Austria Gmbh
  • FDA Inspection 1301512 - 2025-05-23
  • FDA Inspection 1199272 - 2021-07-15
  • FDA Inspection 1110698 - 2018-09-27
  • FDA Inspection 906758 - 2014-11-07
  • FDA Inspection 741633 - 2011-07-29

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