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FUJISAWA SHOJI CO.,LTD.

FDA Regulatory Profile

FUJISAWA SHOJI CO.,LTD. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Feb 16, 2018 · 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
Inspections3Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 16, 2018Gyoda, JapanFood/CosmeticsVoluntary Action Indicated (VAI)3009885774
Feb 3, 2015Saitama, JapanFood/CosmeticsNo Action Indicated (NAI)1000385000
Sep 6, 2011Saitama, JapanFood/CosmeticsVoluntary Action Indicated (VAI)1000385000

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 3009885774Gyoda, Japan1Feb 16, 2018
FEI 1000385000Saitama, Japan2Feb 3, 2015

FDA data resources

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