WONILBIO CO.,LTD

FDA Regulatory Profile

WONILBIO CO.,LTD has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "WONILBIO CO.,LTD" and its spelling variant "Wonilbio Co".

Latest inspection
Oct 25, 2024 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

2 inspections on Oct 25, 2024.

DateSiteProductClassificationFEI
Oct 25, 2024Jecheon, Korea (The Republic Of)Food/CosmeticsNo Action Indicated (NAI)3027684702
Oct 25, 2024Jecheon, Korea (The Republic Of)Food/CosmeticsNo Action Indicated (NAI)3010351406

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.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3010351406Jecheon, Korea (The Republic Of)1Oct 25, 2024
FEI 3027684702Jecheon, Korea (The Republic Of)1Oct 25, 2024

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