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Sol-Ti, Inc.

FDA Regulatory Profile

Sol-Ti, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jan 30, 2026 · 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 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 30, 2026San Diego, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013414473
Sep 12, 2024San Diego, CAFood/CosmeticsNo Action Indicated (NAI)3013414473
Oct 5, 2023San Diego, CAVeterinaryNo Action Indicated (NAI)3013414473
Feb 8, 2023San Diego, CAVeterinaryVoluntary Action Indicated (VAI)3013414473

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 3013414473San Diego, CA4Jan 30, 2026

FDA data resources

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