FDA Inspection 1105180 - Swedish Orphan Biovitrum AB (Publ) - August 29, 2019

FDA Inspection 1105180 for Swedish Orphan Biovitrum AB (Publ) on August 29, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1105180 for Swedish Orphan Biovitrum AB (Publ) on August 29, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

Swedish Orphan Biovitrum AB (Publ)

Inspection Date

August 29, 2019

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fa4d0b7b-782d-4ed1-9f67-03bcd82cb8d2

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