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FDA Inspection
•Arevipharma GmbH•September 16, 2019

Arevipharma GmbH – FDA Inspection, Sep 16, 2019

Record Details

This FDA Inspection record concerns Arevipharma GmbH, with an inspection on September 16, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Arevipharma GmbH
Inspection Date
September 16, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • MRA McCulloughJ (Issuing Officer)
View Company Profile

ID · d795ea7c-d802-42db-ae9e-0fbc04a1d9ab

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1141793
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Arevipharma GmbH

4
DateClassificationOfficeProject area
June 20, 2025Not classifiedOffice of Inspections and Investigations
April 29, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 16, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 8, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Arevipharma GmbH
  • FDA Inspection 1288700 - 2025-06-20
  • FDA Inspection 969875 - 2016-04-29
  • FDA Inspection 808573 - 2012-11-16
  • FDA Inspection 576014 - 2009-04-08

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