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FDA Inspection
•Siegfried PharmaChemikalien Minden Gmbh•March 8, 2019

Siegfried PharmaChemikalien Minden Gmbh – FDA Inspection, Mar 8, 2019

Record Details

This FDA Inspection record concerns Siegfried PharmaChemikalien Minden Gmbh, with an inspection on March 8, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Siegfried PharmaChemikalien Minden Gmbh
Inspection Date
March 8, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Alan P. Kurtzberg (FDA Associated Person)
View Company Profile

ID · c606b926-535b-45f7-bd4e-40e89ae7a1c2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1082891
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Siegfried PharmaChemikalien Minden Gmbh

4
DateClassificationOfficeProject area
April 21, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 3, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 24, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 10, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Siegfried PharmaChemikalien Minden Gmbh
  • FDA Inspection 1265456 - 2023-04-21
  • FDA Inspection 1003148 - 2017-02-03
  • FDA Inspection 909367 - 2014-10-24
  • FDA Inspection 771815 - 2012-02-10

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