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VISVITA CORPORATION

FDA Regulatory Profile

VISVITA CORPORATION has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jul 17, 2026 · NAI

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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
Inspections5Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 17, 2026Fullerton, CAFood/CosmeticsNo Action Indicated (NAI)3013596761
Dec 8, 2023Fullerton, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013596761
May 25, 2023Fullerton, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013596761
Apr 26, 2022Fullerton, CAFood/CosmeticsOfficial Action Indicated (OAI)3013596761
Jul 17, 2019Fullerton, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013596761

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 3013596761Fullerton, CA5Jul 17, 2026

FDA data resources

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