Lone Palm, Inc.

FDA Regulatory Profile

Lone Palm, Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 25, 2025 · VAI

Reviewing Lone Palm, 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 Lone Palm, 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
Inspections8Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 25, 2025Hawi, HIFood/CosmeticsVoluntary Action Indicated (VAI)1000101405
Jun 16, 2022Hawi, HIFood/CosmeticsVoluntary Action Indicated (VAI)1000101405
Nov 30, 2018Hawi, HIFood/CosmeticsOfficial Action Indicated (OAI)1000101405
Feb 7, 2018Hawi, HIFood/CosmeticsOfficial Action Indicated (OAI)1000101405
Mar 23, 2017Hawi, HIFood/CosmeticsNo Action Indicated (NAI)1000101405
Sep 11, 2014Hawi, HIFood/CosmeticsNo Action Indicated (NAI)1000101405
Jul 6, 2011Hawi, HIFood/CosmeticsNo Action Indicated (NAI)1000101405
Sep 7, 2010Hawi, HIFood/CosmeticsVoluntary Action Indicated (VAI)1000101405

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 1000101405Hawi, HI8Jun 25, 2025

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