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Sanford Reproductive Medicine FDA Inspection Record

FEI 3005043101 · Inspections, Form 483s, warning letters and import refusals

Sanford Reproductive Medicine is an FDA-inspected facility (FEI 3005043101) located in Fargo, ND, US. RegDataLab tracks 6 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 30, 2025: No Action Indicated (NAI)
Inspections on record
6 (6 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
Apr 30, 2025No Action Indicated (NAI)No citations listed
May 31, 2022No Action Indicated (NAI)No citations listed
Aug 14, 2017No Action Indicated (NAI)No citations listed
Sep 23, 2014No Action Indicated (NAI)No citations listed
Dec 21, 2011No Action Indicated (NAI)No citations listed
Aug 2, 2010No Action Indicated (NAI)No citations listed

Facility details

Company
Sanford Reproductive Medicine
Location
Fargo, ND (US)
Source
inspections

FDA data resources

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