# Ionetix Corporation – FDA Inspection, Jul 12, 2019

Source: https://www.keypedia.com/records/fda_inspections/ionetix-corporation/31b54cf0-6673-4711-babd-adfa4015dc3b
Source feed: FDA_Inspections

> FDA inspection 1097847 of Ionetix Corporation, July 12, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 212. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097847
- Company Name: Ionetix Corporation
- Inspection Date: 2019-07-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Generic Drug Evaluation
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Kansas City District Office
- Citation Count: 3

## Related Documents

- [FDA Inspection 1289498 - 2025-10-31](https://www.keypedia.com/records/fda_inspections/ionetix-corporation/5c9b34a1-6c89-4161-93b9-ba815a4b0338)
- FDA Inspection 1137344 - 2021-02-25

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/zachary-l-stamm/b729fab9-4d31-4c70-b5b3-e8b6207769c6)

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

Office: https://www.keypedia.com/offices/kansas-city-district-office/cd397ab1-df4e-46f1-ab1c-0f6db9abcf79