Thymoorgan Pharmazie Gmbh | FDA | Inspections | Form 483 | Warning Letters | PharmaCompass.com

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2 FDA, 1 GDUFA

2 FDA
1 GDUFA

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01 2Thymoorgan Pharmazie 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 12014-05-22

02 12010-02-09

filter City Reset all filters

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01 2Vienenburg

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01 2DE

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FDA Audited

USA

euroPLX 86 Munich

Not Confirmed

FDA Audited

USA

euroPLX 86 Munich

Not Confirmed

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District Decision : Voluntary Action Indicated

Inspection End Date : 2010-02-09

Thymoorgan Pharmazie GmbH

City : Vienenburg

State :

Country/Area : DE

Zip :

District : ORA

Center : CDER

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2010-02-09

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#PipelineProspector

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02

FDA Audited

USA

euroPLX 86 Munich

Not Confirmed

FDA Audited

USA

euroPLX 86 Munich

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 : 2014-05-22

Thymoorgan Pharmazie GmbH

City : Vienenburg

State :

Country/Area : DE

Zip :

District : ORA

Center : CDER

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2014-05-22

Product
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Stock Recap
#PipelineProspector

Data Compilation
#PharmaFlow

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