Holy Land Brand Inc.

FDA Regulatory Profile

Holy Land Brand Inc. has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Oct 15, 2021 · VAI

Reviewing Holy Land Brand Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Holy Land Brand Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections9Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 15, 2021Minneapolis, MNFood/CosmeticsVoluntary Action Indicated (VAI)3013439486
Mar 21, 2019Minneapolis, MNFood/CosmeticsNo Action Indicated (NAI)3007272999
Oct 25, 2018Minneapolis, MNFood/CosmeticsVoluntary Action Indicated (VAI)3013439486
Mar 9, 2018Minneapolis, MNFood/CosmeticsOfficial Action Indicated (OAI)3013439486
Apr 19, 2017Minneapolis, MNFood/CosmeticsVoluntary Action Indicated (VAI)3013439486
Apr 18, 2016Minneapolis, MNFood/CosmeticsVoluntary Action Indicated (VAI)3007272999
Jul 28, 2015Minneapolis, MNFood/CosmeticsVoluntary Action Indicated (VAI)3007272999
Nov 15, 2013Minneapolis, MNFood/CosmeticsVoluntary Action Indicated (VAI)3007272999
Nov 1, 2010Minneapolis, MNFood/CosmeticsNo Action Indicated (NAI)3007272999

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3013439486Minneapolis, MN4Oct 15, 2021
FEI 3007272999Minneapolis, MN5Mar 21, 2019

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