Home / Facilities / 3017953815

Ionetix Corporation — FDA Facility Profile

FEI 3017953815

Ionetix Corporation is an FDA-registered facility (FEI 3017953815) located in Miami, FL, US. Registered operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION. RegDataLab tracks 1 FDA inspection at this facility.

Reviewing Ionetix Corporation as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Ionetix Corporation yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

What FDA found at this site

Latest inspection
May 1, 2025: Voluntary Action Indicated (VAI)
Inspections on record
1 (1 VAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
May 1, 2025Voluntary Action Indicated (VAI)Lack Adequate Resources, Facilities, Equipment. (21 CFR 212.10)
Analytical methods (21 CFR 212.60(c))
Correction of problems (21 CFR 212.71(c))
Equipment procedures (21 CFR 212.30(b))
and 1 more

Facility details

Company
Ionetix Corporation
Location
Miami, FL (US)
Registration Expires
Dec 31, 2027
Operations
POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION
Source
decrs

FDA data resources

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