# Ionetix Corporation, Kansas City, KS – FDA Inspections

Source: https://www.keypedia.com/companies/ionetix-corporation/a014fcbf-0e12-434a-bb00-adb100627897

> Inspection records and compliance data for Ionetix Corporation in Kansas City, Kansas. 3 FDA inspections on record, 2 Form 483s, last inspected October 31, 2025.

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## Details

- Name: Ionetix Corporation
- FEI Number: 3015265824
- Business Operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION
- Address Line 1: 3901 Rainbow Blvd Ste B701
- City: Kansas City
- State: Kansas
- Zip Code: 66103
- Country Name: United States
- Address: 3901 Rainbow Blvd Ste B701, Kansas City, Kansas 66103, United States
- Country: United States

## Related Documents

- [483 - Ionetix Corporation - 2025-10-31](https://www.keypedia.com/records/483/ionetix-corporation/a6d87a79-ea3c-44a0-a6c9-1783a09f1361) — source: FDA, date: October 31, 2025
- [FDA Inspection 1289498 - Ionetix Corporation - 2025-10-31](https://www.keypedia.com/records/fda_inspections/ionetix-corporation/5c9b34a1-6c89-4161-93b9-ba815a4b0338) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2025
- FDA Inspection 1137344 - Ionetix Corporation - 2021-02-25 — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2021
- [483 - Ionetix Corporation - 2019-07-12](https://www.keypedia.com/records/483/ionetix-corporation/2d06477e-fa6f-46a4-81b9-10fe4479c948) — source: FDA, date: July 12, 2019
- [FDA Inspection 1097847 - Ionetix Corporation - 2019-07-12](https://www.keypedia.com/records/fda_inspections/ionetix-corporation/31b54cf0-6673-4711-babd-adfa4015dc3b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2019

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