Cytovance Biologics | FDA | Inspections | Form 483 | Warning Letters | PharmaCompass.com

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Cytovance Biologics
FDA

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Cytovance Biologics

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INSPECTIONS & REGISTRATIONS

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01 2Cytovance Biologics Inc.

filter District Decision Reset all filters

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01 1No Action Indicated

02 1Voluntary Action Indicated

filter Inspection End Date Reset all filters

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01 12019-05-09

02 12017-07-20

filter City Reset all filters

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01 2Oklahoma City

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01 2U.S.A

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FDA Audited

USA

IPPE

Not Confirmed

FDA Audited

USA

IPPE

Not Confirmed

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District Decision : No Action Indicated

Inspection End Date : 2019-05-09

Cytovance Biologics

City : Oklahoma City

State : Oklahoma

Country/Area : U.S.A

Zip : 73104

District :

Center :

Project Area : Drug Quality Assurance

District Decision : No Action Indicated

Inspection End Date : 2019-05-09

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Data Compilation
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02

FDA Audited

USA

IPPE

Not Confirmed

FDA Audited

USA

IPPE

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 : 2017-07-20

Cytovance Biologics

City : Oklahoma City

State : Oklahoma

Country/Area : U.S.A

Zip : 73104

District :

Center :

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2017-07-20

Product
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Stock Recap
#PipelineProspector

Data Compilation
#PharmaFlow

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