Laboratorio Reig Jofre S.A.

FDA Regulatory Profile

Laboratorio Reig Jofre S.A. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 23, 2023 · OAI

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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 actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 23, 2023Toledo, SpainDrugsOfficial Action Indicated (OAI)3009713694
Apr 5, 2019Sant Joan Despi, SpainDrugsOfficial Action Indicated (OAI)3003768199
Jul 24, 2015Sant Joan Despi, SpainDrugsOfficial Action Indicated (OAI)3003768199
Jul 14, 2015Toledo, SpainDrugsOfficial Action Indicated (OAI)3009713694
Jul 31, 2013Toledo, SpainDrugsVoluntary Action Indicated (VAI)3009713694

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 3009713694Toledo, Spain3Jun 23, 2023
FEI 3003768199Sant Joan Despi, Spain2Apr 5, 2019

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