Nevada Donor Network Inc FDA Inspection Record

FEI 3000718306 · Inspections, Form 483s, warning letters and import refusals

Nevada Donor Network Inc is an FDA-inspected facility (FEI 3000718306) located in Las Vegas, NV, US. RegDataLab tracks 6 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 17, 2025: Voluntary Action Indicated (VAI)
Inspections on record
6 (3 VAI, 3 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
Recalls as the recalling firm
6, latest Oct 20, 2022

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 17, 2025Voluntary Action Indicated (VAI)Donors with risks not determined ineligible (21 CFR 1271.75(d))
Jul 13, 2022No Action Indicated (NAI)No citations listed
Jul 20, 2017No Action Indicated (NAI)No citations listed
Jan 27, 2014No Action Indicated (NAI)No citations listed
Mar 14, 2012Voluntary Action Indicated (VAI)No citations listed
Aug 20, 2009Voluntary Action Indicated (VAI)No citations listed

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Oct 20, 2022Class IIB-0214-2023Sclera
Sclera, in which donor testing was conducted with an unacceptable sample, was distributed.
Mar 16, 2022Class IIB-0333-2022Cornea
Corneas, recovered from a donor in which donor suitability was not adequately determined, were distributed.
Jul 3, 2019Class IIB-0216-2020Cornea; Cornea; long term tectonic preservation in medium 200 proof, 99.5% Ethyl Alcohol…
Long term preserved corneal tissues, processed in a manner that could cause contamination or cross-contamination during processing, as well…
Jul 3, 2019Class IIB-0217-2020Cornea; long term tectonic preservation in medium 200 proof, 99.5% Ethyl Alcohol. Not…
Long term preserved corneal tissues, processed in a manner that could cause contamination or cross-contamination during processing, as well…
Jul 3, 2019Class IIB-0218-2020Cornea; long term tectonic preservation in medium 200 proof, 99.5% Ethyl Alcohol. Not…
Long term preserved corneal tissues, processed in a manner that could cause contamination or cross-contamination during processing, as well…
Jul 3, 2019Class IIB-0219-2020Cornea; long term tectonic preservation in medium 200 proof, 99.5% Ethyl Alcohol. Not…
Long term preserved corneal tissues, processed in a manner that could cause contamination or cross-contamination during processing, as well…

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Nevada Donor Network Inc
Location
Las Vegas, NV (US)
Source
inspections

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