FDA Inspection 1148996 — Ionetix Corporation

Ionetix Corporation — FEI 3015287791

The FDA completed an inspection of Ionetix Corporation on Jun 30, 2021 in Jenkintown, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 30, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jenkintown, PA (United States)

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