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FDA Inspection
•Wasserburger Arzneimittelwerk GmbH•September 10, 2013

FDA Inspection 852201 - Wasserburger Arzneimittelwerk GmbH - September 10, 2013

Record Details

This FDA Inspection record concerns Wasserburger Arzneimittelwerk GmbH, with an inspection on September 10, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Wasserburger Arzneimittelwerk GmbH
Inspection Date
September 10, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 49aa197e-a421-417a-b1bc-3548f85481cc

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
852201
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Wasserburger Arzneimittelwerk GmbH

4
DateClassificationOfficeProject area
May 2, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 23, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 27, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 9, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Wasserburger Arzneimittelwerk GmbH
  • FDA Inspection 1240649 - 2024-05-02
  • FDA Inspection 1039842 - 2018-01-23
  • FDA Inspection 947759 - 2015-10-27
  • FDA Inspection 703289 - 2010-11-09

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