Frontida Biopharm | FDA | Inspections | Form 483 | Warning Letters | PharmaCompass.com

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INSPECTIONS & REGISTRATIONS

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01 2Frontida BioPharm 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 12017-07-20

02 12017-03-31

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01 2Philadelphia

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01 2US

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01

FDA Audited

USA

Antibody Engineering

Not Confirmed

FDA Audited

USA

Antibody Engineering

Not Confirmed

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District Decision : Voluntary Action Indicated

Inspection End Date : 2017-03-31

Frontida BioPharm

City : Philadelphia

State : PA

Country/Area : US

Zip : 19124-3168

District : PHI

Center : CDER

Project Area : Drug Quality Assurance

District Decision : Voluntary Action Indicated

Inspection End Date : 2017-03-31

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#PipelineProspector

Data Compilation
#PharmaFlow

02

FDA Audited

USA

Antibody Engineering

Not Confirmed

FDA Audited

USA

Antibody Engineering

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 : No Action Indicated

Inspection End Date : 2017-07-20

Frontida BioPharm

City : Philadelphia

State : PA

Country/Area : US

Zip : 19111-2733

District : PHI

Center : CDER

Project Area : Drug Quality Assurance

District Decision : No Action Indicated

Inspection End Date : 2017-07-20

Product
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Stock Recap
#PipelineProspector

Data Compilation
#PharmaFlow

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