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FDA Inspection
•Siegfried (St. Vulbas) SAS•September 23, 2016

Siegfried (St. Vulbas) SAS – FDA Inspection, Sep 23, 2016

Record Details

This FDA Inspection record concerns Siegfried (St. Vulbas) SAS, with an inspection on September 23, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Siegfried (St. Vulbas) SAS
Inspection Date
September 23, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 96026e0b-8591-41bc-956f-a11d10d5f804

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
990166
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Siegfried (St. Vulbas) SAS

5
DateClassificationOfficeProject area
January 13, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 7, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 29, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 18, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 22, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Siegfried (St. Vulbas) SAS
  • FDA Inspection 1247255 - 2023-01-13
  • FDA Inspection 1125537 - 2019-11-07
  • FDA Inspection 1063219 - 2018-06-29
  • FDA Inspection 889637 - 2013-12-18
  • FDA Inspection 645432 - 2010-01-22

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