Hameln Pharma Gmbh | FDA | Inspections | Form 483 | Warning Letters | PharmaCompass.com

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Hameln Pharma GmbH
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Hameln Pharma GmbH

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FINISHED DOSAGE FORMULATIONS

41 FDF Dossiers, 41 Europe

41 FDF Dossiers
41 Europe

INSPECTIONS & REGISTRATIONS

2 FDA, 6 EDQM, 1 GDUFA

2 FDA
6 EDQM
1 GDUFA

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01 2Hameln Pharmaceuticals Gmbh

filter District Decision Reset all filters

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01 2Voluntary Action Indicated

filter Inspection End Date Reset all filters

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01 12014-07-25

02 12009-11-09

filter City Reset all filters

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01 2Hameln

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01 2DE

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01

FDA Audited

USA

Medlab Asia & Asia Health

Not Confirmed

FDA Audited

USA

Medlab Asia & Asia Health

Not Confirmed

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District Decision : Voluntary Action Indicated

Inspection End Date : 2009-11-09

Hameln Pharma GmbH

City : Hameln

State :

Country/Area : DE

Zip :

District : ORA

Center : CDER

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2009-11-09

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#PipelineProspector

Data Compilation
#PharmaFlow

02

FDA Audited

USA

Medlab Asia & Asia Health

Not Confirmed

FDA Audited

USA

Medlab Asia & Asia Health

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

District Decision : Voluntary Action Indicated

Inspection End Date : 2014-07-25

Hameln Pharma GmbH

City : Hameln

State :

Country/Area : DE

Zip :

District : ORA

Center : CDER

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2014-07-25

Product
Web Link

Stock Recap
#PipelineProspector

Data Compilation
#PharmaFlow

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