FDA Inspection 1050664 - Swedish Orphan Biovitrum AB (Publ) - May 04, 2018

FDA Inspection 1050664 for Swedish Orphan Biovitrum AB (Publ) on May 04, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1050664 for Swedish Orphan Biovitrum AB (Publ) on May 04, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.198(a)

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Record Information

Company

Swedish Orphan Biovitrum AB (Publ)

Inspection Date

May 4, 2018

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fedd8529-51b4-48a4-a3ce-9099fcb8a7d3

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