FDA Inspection 1327528 — Ionetix Corporation

Ionetix Corporation — FEI 3015287791

The FDA completed an inspection of Ionetix Corporation on Jul 23, 2026 in Jenkintown, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 23, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jenkintown, PA (United States)

Citations

IDCFRDescription
1794021 CFR 212.71(a)Non-Conforming Product Investigation Incomplete

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.