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FDA Inspection
•R-Pharm Germany GmbH•November 7, 2014

R-Pharm Germany GmbH – FDA Inspection, Nov 7, 2014

Record Details

This FDA Inspection record concerns R-Pharm Germany GmbH, with an inspection on November 7, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
R-Pharm Germany GmbH
Inspection Date
November 7, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 202801ae-b182-44a9-9de2-c55c4d8c4190

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
904022
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of R-Pharm Germany GmbH

4
DateClassificationOfficeProject area
February 28, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 1, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 10, 2017Not classifiedOffice of Inspections and Investigations
June 18, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for R-Pharm Germany GmbH
  • FDA Inspection 1268201 - 2023-02-28
  • FDA Inspection 1111807 - 2019-08-01
  • FDA Inspection 1001146 - 2017-02-10
  • FDA Inspection 673156 - 2010-06-18

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