Herbrand PharmaChemicals GmbH
FDA Inspections Database

Herbrand PharmaChemicals GmbH

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 2022-12-09
  • Data Source U.S. FDA
  • Last Updated 2023-02-15
Company Overview

Company

Herbrand PharmaChemicals GmbH

Country

Germany

Social Profiles

Company Snapshot

Herbrand PharmaChemicals GmbH

Brambachstraße 31 77723 Gengenbach Germany

Germany

herbrand-hpc.de/ info@herbrand-hpc.de View on Map
FDA Inspections Timeline (3 records)
2022
09 Dec
Voluntary Action Indicated VAI

Legal Name

Herbrand PharmaChemicals GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2022-12-09

FMD Date

2023-02-15

Fiscal Year

2023

State

Gengenbach, Germany

Location

Gengenbach, , Germany

Inspection Info

Fiscal Year: 2023
Citations: No

2016
17 Jun
Voluntary Action Indicated VAI

Legal Name

Herbrand PharmaChemicals GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2016-06-17

FMD Date

2016-09-30

Fiscal Year

2016

State

Gengenbach, Germany

Location

Gengenbach, , Germany

Inspection Info

Fiscal Year: 2016
Citations: No

2012
15 Jun
Voluntary Action Indicated VAI

Legal Name

Herbrand PharmaChemicals GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2012-06-15

FMD Date

2012-10-24

Fiscal Year

2012

State

Gengenbach, Germany

Location

Gengenbach, , Germany

Inspection Info

Fiscal Year: 2012
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

Gengenbach, , Germany

Inspection Info

Fiscal Year: 2023
Citations: No

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

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