FDA Inspection 1218250 - Octapharma AB - September 19, 2023

FDA Inspection 1218250 for Octapharma AB on September 19, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1218250 for Octapharma AB on September 19, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.100(b)

21 CFR 211.110(a)

21 CFR 211.67(a)

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Record Information

Company

Octapharma AB

Inspection Date

September 19, 2023

Product Type

Biologics

Office

Center for Biologics Evaluation and Research

ID: 3645f477-d675-40fc-90b8-3704a595408d

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