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Nippon Rika Co., Ltd.

FDA Regulatory Profile

Nippon Rika Co., Ltd. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 4, 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
Inspections4Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 4, 2025Ashikaga, JapanDrugsVoluntary Action Indicated (VAI)3002807731
Aug 9, 2018Ashikaga, JapanDrugsNo Action Indicated (NAI)3002807731
Feb 13, 2015Ashikaga, JapanDrugsVoluntary Action Indicated (VAI)3002807731
Sep 22, 2011Ashikaga, JapanDrugsVoluntary Action Indicated (VAI)3002807731

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 3002807731Ashikaga, Japan4Jul 4, 2025

FDA data resources

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