NextPharma Technologies Holding Ltd
FDA Inspections Database

NextPharma Technologies Holding Ltd

FDA Inspections Database

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

VAI · Voluntary Action IndicatedNAI · No Action Indicated Germany
  • Total Records 14
  • Latest Inspection 2025-06-06
  • Data Source U.S. FDA
  • Last Updated 2025-08-06

14

All
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1

NAI
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13

VAI
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Company Overview

Company

NextPharma Technologies Holding Ltd

Country

United Kingdom

Social Profiles

Company Snapshot

NextPharma Technologies Holding Ltd

Connaught House, Portsmouth Road

United Kingdom

nextpharma.com/ info@nextpharma.com View on Map
FDA Inspections Timeline (14 records)
2025
06 Jun
Voluntary Action Indicated VAI

Legal Name

Pharbil Waltrop Gmbh

Project Area

Pre-Approval Eval. of Animal Drugs and Food Additives

Product Type

Veterinary

Posted Citations

Yes

Inspection End Date

2025-06-06

FMD Date

2025-08-06

Fiscal Year

2025

State

Waltrop, Germany

Location

Waltrop, , Germany

Inspection Info

Fiscal Year: 2025
Citations: Yes

2024
19 Nov
Voluntary Action Indicated VAI

Legal Name

allphamed PHARBIL Arzneimittel GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2024-11-19

FMD Date

-

Fiscal Year

2025

State

Gottingen, Germany

Additional Details

Mutual Recognition Agreement (MRA)

Location

Gottingen, , Germany

Inspection Info

Fiscal Year: 2025
Citations: No

2023
27 Sep
Voluntary Action Indicated VAI

Legal Name

PenCef Pharma GmbH

Project Area

Pre-Approval Eval. of Animal Drugs and Food Additives

Product Type

Veterinary

Posted Citations

Yes

Inspection End Date

2023-09-27

FMD Date

2023-11-27

Fiscal Year

2023

State

Berlin, Germany

Location

Berlin, , Germany

Inspection Info

Fiscal Year: 2023
Citations: Yes

2020
01 Oct
Voluntary Action Indicated VAI

Legal Name

allphamed PHARBIL Arzneimittel GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2020-10-01

FMD Date

2021-04-29

Fiscal Year

2021

State

Gottingen, Germany

Additional Details

Mutual Recognition Agreement (MRA)

Location

Gottingen, , Germany

Inspection Info

Fiscal Year: 2021
Citations: No

2020
14 Feb
Voluntary Action Indicated VAI

Legal Name

Pharbil Waltrop Gmbh

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

Yes

Inspection End Date

2020-02-14

FMD Date

2020-04-03

Fiscal Year

2020

State

Waltrop, Germany

Location

Waltrop, , Germany

Inspection Info

Fiscal Year: 2020
Citations: Yes

2020
14 Feb
Voluntary Action Indicated VAI

Legal Name

Pharbil Waltrop Gmbh

Project Area

Monitoring of Marketed Animal Drugs, Feed, and Devices

Product Type

Veterinary

Posted Citations

Yes

Inspection End Date

2020-02-14

FMD Date

2020-04-03

Fiscal Year

2020

State

Waltrop, Germany

Location

Waltrop, , Germany

Inspection Info

Fiscal Year: 2020
Citations: Yes

2018
22 Jun
Voluntary Action Indicated VAI

Legal Name

Pharbil Waltrop Gmbh

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

Yes

Inspection End Date

2018-06-22

FMD Date

2018-10-15

Fiscal Year

2018

State

Waltrop, Germany

Location

Waltrop, , Germany

Inspection Info

Fiscal Year: 2018
Citations: Yes

2017
29 Sep
Voluntary Action Indicated VAI

Legal Name

allphamed PHARBIL Arzneimittel GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2017-09-29

FMD Date

2018-01-26

Fiscal Year

2017

State

Gottingen, Germany

Location

Gottingen, , Germany

Inspection Info

Fiscal Year: 2017
Citations: No

2017
12 May
Voluntary Action Indicated VAI

Legal Name

PenCef Pharma GmbH

Project Area

Pre-Approval Eval. of Animal Drugs and Food Additives

Product Type

Veterinary

Posted Citations

No

Inspection End Date

2017-05-12

FMD Date

-

Fiscal Year

2017

State

Berlin, Germany

Location

Berlin, , Germany

Inspection Info

Fiscal Year: 2017
Citations: No

2015
10 Jul
Voluntary Action Indicated VAI

Legal Name

allphamed PHARBIL Arzneimittel GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2015-07-10

FMD Date

2015-10-08

Fiscal Year

2015

State

Gottingen, Germany

Location

Gottingen, , Germany

Inspection Info

Fiscal Year: 2015
Citations: No

2014
05 Sep
Voluntary Action Indicated VAI

Legal Name

allphamed PHARBIL Arzneimittel GmbH

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2014-09-05

FMD Date

2014-11-17

Fiscal Year

2014

State

Gottingen, Germany

Location

Gottingen, , Germany

Inspection Info

Fiscal Year: 2014
Citations: No

2014
24 Jan
No Action Indicated NAI

Legal Name

Pharbil Waltrop Gmbh

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2014-01-24

FMD Date

2014-06-05

Fiscal Year

2014

State

Waltrop, Germany

Location

Waltrop, , Germany

Inspection Info

Fiscal Year: 2014
Citations: No

2008
30 Oct
Voluntary Action Indicated VAI

Legal Name

Pharbil Waltrop Gmbh

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2008-10-30

FMD Date

2008-10-28

Fiscal Year

2009

State

Waltrop, Germany

Location

Waltrop, , Germany

Inspection Info

Fiscal Year: 2009
Citations: No

2008
30 Oct
Voluntary Action Indicated VAI

Legal Name

Pharbil Waltrop Gmbh

Project Area

Pre-Approval Eval. of Animal Drugs and Food Additives

Product Type

Veterinary

Posted Citations

No

Inspection End Date

2008-10-30

FMD Date

2008-10-28

Fiscal Year

2009

State

Waltrop, Germany

Location

Waltrop, , Germany

Inspection Info

Fiscal Year: 2009
Citations: No

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Classification Breakdown
14 total
  • VAI (Voluntary Action Indicated)
  • NAI (No 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

Waltrop, , Germany

Inspection Info

Fiscal Year: 2025
Citations: Yes

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

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