Midwest Transplant Network FDA Inspection Record

FEI 3001238375 · Inspections, Form 483s, warning letters and import refusals

Midwest Transplant Network is an FDA-inspected facility (FEI 3001238375) located in Westwood, KS, US. RegDataLab tracks 12 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 25, 2025: No Action Indicated (NAI)
Inspections on record
12 (2 VAI, 10 NAI)
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

Showing the 10 most recent of 12 inspections. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 25, 2025No Action Indicated (NAI)No citations listed
Feb 19, 2019Voluntary Action Indicated (VAI)Calibration procedures and schedules (general) (21 CFR 1271.200(c))
Cleaned, sanitized per established schedules (21 CFR 1271.200(a))
Lot documentation maintained (21 CFR 1271.210(d)(3))
Potential problems with recovery (21 CFR 1271.215)
Sep 13, 2018No Action Indicated (NAI)No citations listed
Aug 25, 2016No Action Indicated (NAI)No citations listed
Jun 2, 2014No Action Indicated (NAI)No citations listed
Jun 2, 2014No Action Indicated (NAI)No citations listed
Mar 28, 2012No Action Indicated (NAI)No citations listed
Mar 28, 2012No Action Indicated (NAI)No citations listed
Mar 29, 2010No Action Indicated (NAI)No citations listed
Mar 16, 2010No Action Indicated (NAI)No citations listed

Facility details

Company
Midwest Transplant Network
Location
Westwood, KS (US)
Source
inspections

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