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Thai Kee Corporation

FDA Regulatory Profile

Thai Kee Corporation has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
May 21, 2024 · 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
Inspections5Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 21, 2024Antioch, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000161889
Apr 13, 2022Antioch, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000161889
Aug 28, 2020Antioch, CAFood/CosmeticsOfficial Action Indicated (OAI)1000161889
Sep 28, 2017Antioch, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000161889
Sep 14, 2017Antioch, CAFood/CosmeticsNo Action Indicated (NAI)1000161889

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 1000161889Antioch, CA5May 21, 2024

FDA data resources

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