FDA Inspection 1137344 — Ionetix Corporation

Ionetix Corporation — FEI 3015265824

The FDA completed an inspection of Ionetix Corporation on February 25, 2021 in Kansas City, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 25, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, KS (United States)