Pharmachemie B.V. - VAI
FDA Inspections Database

Pharmachemie B.V. - VAI

FDA Inspections Database

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

VAI · Voluntary Action Indicated Netherlands
  • Total Records 3
  • Latest Inspection 2024-10-17
  • Data Source U.S. FDA
  • Last Updated -

6

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3

NAI
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3

VAI
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Company Overview

Company

Pharmachemie B.V. - VAI

Country

Netherlands

Social Profiles

Company Snapshot

Pharmachemie B.V. - VAI

Swensweg 5. P.O. Box 552. 2003 RN Haarlem

Netherlands

www.tevapharmachemie.com/ pch.servicedesk@tevanederland.com View on Map
FDA Inspections Timeline (3 records)
2024
17 Oct
Voluntary Action Indicated VAI

Legal Name

Pharmachemie B.V.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2024-10-17

FMD Date

-

Fiscal Year

2025

State

Haarlem, Netherlands

Additional Details

Mutual Recognition Agreement (MRA)

Location

Haarlem, , Netherlands

Inspection Info

Fiscal Year: 2025
Citations: No

2013
28 Jun
Voluntary Action Indicated VAI

Legal Name

Pharmachemie B.V.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

Yes

Inspection End Date

2013-06-28

FMD Date

2013-09-12

Fiscal Year

2013

State

Haarlem, Netherlands

Location

Haarlem, , Netherlands

Inspection Info

Fiscal Year: 2013
Citations: Yes

2010
19 Feb
Voluntary Action Indicated VAI

Legal Name

Pharmachemie B.V.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2010-02-19

FMD Date

2010-07-08

Fiscal Year

2010

State

Haarlem, Netherlands

Location

Haarlem, , Netherlands

Inspection Info

Fiscal Year: 2010
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

Haarlem, , Netherlands

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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