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Dae Shin Mul San Co., Ltd.

FDA Regulatory Profile

Dae Shin Mul San Co., Ltd. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 3, 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
Inspections2Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 3, 2025Gimhae, Korea (The Republic Of)Food/CosmeticsVoluntary Action Indicated (VAI)3014859581
Jun 12, 2015Gimhae-Si, Korea (The Republic Of)Food/CosmeticsVoluntary Action Indicated (VAI)3009914564

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 3014859581Gimhae, Korea (The Republic Of)1Dec 3, 2025
FEI 3009914564Gimhae-Si, Korea (The Republic Of)1Jun 12, 2015

FDA data resources

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