FDA Inspection 1283830 - Ionetix Corporation - September 26, 2025

FDA Inspection 1283830 for Ionetix Corporation on September 26, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1283830 for Ionetix Corporation on September 26, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 212.10

21 CFR 212.20(e)

21 CFR 212.30(a)

21 CFR 212.30(b)

21 CFR 212.40(a)

21 CFR 212.40(c)

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Record Information

Company

Ionetix Corporation

Inspection Date

September 26, 2025

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 854c2365-bc37-4654-8b6e-3ffbe96b6cbc

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