Genvion Corporation | FDA | Inspections | Form 483 | Warning Letters | PharmaCompass.com

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Genvion Corporation
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FAMAR CDMO- From early development to commercial manufacturing.

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Genvion Corporation

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01 2Genvion Corporation

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01 1No Action Indicated

02 1Voluntary Action Indicated

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01 12023-07-28

02 12016-06-17

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01 2Winnipeg

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FDA Audited

USA

34th NZW-Hamburg

Not Confirmed

FDA Audited

USA

34th NZW-Hamburg

Not Confirmed

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District Decision : Voluntary Action Indicated

Inspection End Date : 2023-07-28

Genvion Corporation

City : Winnipeg

State :

Country/Area : Canada

Zip :

District :

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Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2023-07-28

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02

FDA Audited

USA

34th NZW-Hamburg

Not Confirmed

FDA Audited

USA

34th NZW-Hamburg

Not Confirmed

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District Decision : No Action Indicated

Inspection End Date : 2016-06-17

Genvion Corporation

City : Winnipeg

State :

Country/Area : Canada

Zip :

District :

Center :

Project Area : Drug Quality Assurance

District Decision : No Action Indicated

Inspection End Date : 2016-06-17

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Contact Genvion Corporation and get a quotation

Genvion Corporation is a supplier offers 3 products (APIs, Excipients or Intermediates).

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