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Vege Labs LLC. FDA Inspection Record

FEI 3018521591 · Inspections, Form 483s, warning letters and import refusals

Vege Labs LLC. is an FDA-registered facility (FEI 3018521591) located in Glendale, CA, US. Registered operations: MANUFACTURE. RegDataLab tracks 7 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 18, 2025: Voluntary Action Indicated (VAI)
Inspections on record
7 (1 OAI, 6 VAI)
Last OAI inspection
Dec 20, 2011
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 18, 2025Voluntary Action Indicated (VAI)Written procedures not established/followed (21 CFR 211.67(b))
Computer control of master formula records (21 CFR 211.68(b))
Reports of Analysis (Components) (21 CFR 211.84(d)(2))
No written record of investigation (21 CFR 211.192)
Jan 24, 2020Voluntary Action Indicated (VAI)Cleaning SOPs/equipment identification (21 CFR 211.67(b)(4))
Buildings not maintained in good state of repair (21 CFR 211.58)
May 5, 2017Voluntary Action Indicated (VAI)Procedures not in writing, fully followed (21 CFR 211.22(d))
Training--operations, GMPs, written procedures (21 CFR 211.25(a))
Equipment Design, Size and Location (21 CFR 211.63)
Written procedures not established/followed (21 CFR 211.67(b))
and 15 more
Sep 15, 2014Voluntary Action Indicated (VAI)Absence of Written Procedures (21 CFR 211.100(a))
Review of representative number of batches (21 CFR 211.180(e)(1))
Written procedures followed (21 CFR 211.186(a))
Control procedures to monitor and validate performance (21 CFR 211.110(a))
and 2 more
Dec 20, 2011Official Action Indicated (OAI)GMP Training Frequency (21 CFR 211.25(a))
Cleaning / Sanitizing / Maintenance (21 CFR 211.67(a))
Following/documenting laboratory controls (21 CFR 211.160(a))
Control procedures to monitor and validate performance (21 CFR 211.110(a))
and 2 more
Sep 30, 2010Voluntary Action Indicated (VAI)No citations listed
Jun 11, 2009Voluntary Action Indicated (VAI)Control procedures to monitor and validate performance (21 CFR 211.110(a))
Items to cover on annual reviews (21 CFR 211.180(e)(2))

FDA record score

9 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

7 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIMar 18, 20256 x 16
Inspection classified VAIJan 24, 20206 x 0.251.5
Inspection classified VAIMay 5, 20176 x 0.251.5
Inspection classified VAISep 15, 201410 years or older, so it adds no points0
Inspection classified OAIDec 20, 201110 years or older, so it adds no points0
Inspection classified VAISep 30, 201010 years or older, so it adds no points0
Inspection classified VAIJun 11, 200910 years or older, so it adds no points0

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
Vege Labs LLC
Location
Glendale, CA (US)
Registration Expires
Dec 31, 2026
Operations
MANUFACTURE
Source
decrs

FDA data resources

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