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Source-Omega LLC

FDA Regulatory Profile

Source-Omega LLC has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jul 24, 2025 · VAI

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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
Inspections4Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 24, 2025South Lebanon, OHFood/CosmeticsVoluntary Action Indicated (VAI)3014165298
Feb 28, 2024South Lebanon, OHFood/CosmeticsVoluntary Action Indicated (VAI)3014165298
Jan 19, 2023South Lebanon, OHFood/CosmeticsOfficial Action Indicated (OAI)3014165298
Mar 27, 2018South Lebanon, OHFood/CosmeticsVoluntary Action Indicated (VAI)3014165298

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 3014165298South Lebanon, OH4Jul 24, 2025

FDA data resources

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