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Vitalant FDA Inspection Record

FEI 1000123568 · Inspections, Form 483s, warning letters and import refusals

Vitalant is an FDA-inspected facility (FEI 1000123568) located in Auburn, CA, US. RegDataLab tracks 8 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
8 (1 VAI, 7 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 25, 2025No Action Indicated (NAI)No citations listed
May 1, 2019No Action Indicated (NAI)No citations listed
Jul 26, 2017No Action Indicated (NAI)No citations listed
Nov 4, 2014No Action Indicated (NAI)No citations listed
Dec 5, 2012No Action Indicated (NAI)No citations listed
Jun 30, 2011No Action Indicated (NAI)No citations listed
Jul 30, 2009Voluntary Action Indicated (VAI)No citations listed
Dec 3, 2008No Action Indicated (NAI)No citations listed

Facility details

Company
Vitalant
Location
Auburn, CA (US)
Source
inspections

FDA data resources

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