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FDA Inspection
•Fresenius Kabi iPSUM Srl•February 11, 2011

Fresenius Kabi iPSUM Srl – FDA Inspection, Feb 11, 2011

Record Details

This FDA Inspection record concerns Fresenius Kabi iPSUM Srl, with an inspection on February 11, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Fresenius Kabi iPSUM Srl
Inspection Date
February 11, 2011
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 21e4d58d-a28a-47e3-a48e-9ac890078d0d

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
712032
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Fresenius Kabi iPSUM Srl

6
DateClassificationOfficeProject area
January 21, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 6, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 15, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 17, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 27, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Fresenius Kabi iPSUM Srl
  • FDA Inspection 1277643 - 2022-01-21
  • FDA Inspection 1123992 - 2019-12-06
  • FDA Inspection 1078083 - 2017-12-15
  • FDA Inspection 993733 - 2016-11-17
  • FDA Inspection 854585 - 2013-09-27

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