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Midwest Fertility Specialists FDA Inspection Record

FEI 3005620268 · Inspections, Form 483s, warning letters and import refusals

Midwest Fertility Specialists is an FDA-inspected facility (FEI 3005620268) located in Fort Wayne, IN, US. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Mar 22, 2022: No Action Indicated (NAI)
Inspections on record
4 (4 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

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

DateResultWhat FDA cited
Mar 22, 2022No Action Indicated (NAI)No citations listed
Aug 1, 2017No Action Indicated (NAI)No citations listed
Mar 25, 2015No Action Indicated (NAI)No citations listed
Nov 6, 2012No Action Indicated (NAI)No citations listed

Facility details

Company
Midwest Fertility Specialists
Location
Fort Wayne, IN (US)
Source
inspections

FDA data resources

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