Arevipharma - VAI
FDA Inspections Database

Arevipharma - VAI

FDA Inspections Database

U.S. FDA inspection classifications and citation records from the official FDA inspection database.

VAI · Voluntary Action Indicated Germany
  • Total Records 3
  • Latest Inspection 2025-06-20
  • Data Source U.S. FDA
  • Last Updated -

6

All
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3

NAI
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3

VAI
View
Company Overview

Company

Arevipharma - VAI

Country

Germany

Social Profiles

LinkedIn
Company Snapshot

Arevipharma - VAI

Meißner Str. 35 01445 Radebeul

Germany

www.arevipharma.com/ Kerstin.dreissig@arevipharma.com View on Map
FDA Inspections Timeline (3 records)
2025
20 Jun
Voluntary Action Indicated VAI

Legal Name

Arevipharma GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2025-06-20

FMD Date

-

Fiscal Year

2025

State

Radebeul, Germany

Additional Details

Mutual Recognition Agreement (MRA)

Location

Radebeul, , Germany

Inspection Info

Fiscal Year: 2025
Citations: No

2009
08 Apr
Voluntary Action Indicated VAI

Legal Name

Arevipharma GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2009-04-08

FMD Date

2001-03-24

Fiscal Year

2009

State

Radebeul, Germany

Location

Radebeul, , Germany

Inspection Info

Fiscal Year: 2009
Citations: No

2009
08 Apr
Voluntary Action Indicated VAI

Legal Name

Arevipharma GmbH

Project Area

Pre-Approval Eval. of Animal Drugs and Food Additives

Product Type

Veterinary

Posted Citations

No

Inspection End Date

2009-04-08

FMD Date

2001-03-24

Fiscal Year

2009

State

Radebeul, Germany

Location

Radebeul, , Germany

Inspection Info

Fiscal Year: 2009
Citations: No

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Classification Breakdown
3 total
  • VAI (Voluntary Action Indicated)
Official Source

All data is sourced from the official FDA inspection database maintained by the U.S. Food and Drug Administration.

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Location

Radebeul, , Germany

Inspection Info

Fiscal Year: 2025
Citations: No

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FDA inspection data is compiled from publicly available U.S. FDA inspection classification records.

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