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ZULAND DISTRIBUTOR CORP

FDA Regulatory Profile

ZULAND DISTRIBUTOR CORP has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Sep 3, 2024 · OAI

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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
Sep 3, 2024Imperial Beach, CAFood/CosmeticsOfficial Action Indicated (OAI)3014837238
Sep 28, 2023Imperial Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)3014837238
Jul 8, 2022Imperial Beach, CAFood/CosmeticsOfficial Action Indicated (OAI)3014837238
Feb 11, 2021Imperial Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)3014837238

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 3014837238Imperial Beach, CA4Sep 3, 2024

FDA data resources

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