Generitech Corporation

FDA Regulatory Profile

Generitech Corporation has 1 FDA recall, 7 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest recall
D-0111-2025 · Class II · Nov 22, 2024
Latest inspection
Sep 3, 2024 · OAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections7Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
D-0111-2025Class II10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + Science, 1…Nov 22, 2024

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 3, 2024Fresno, CADrugsOfficial Action Indicated (OAI)3002994577
Sep 29, 2023Fresno, CADrugsOfficial Action Indicated (OAI)3002994577
Jul 28, 2021Fresno, CADrugsOfficial Action Indicated (OAI)3002994577
Feb 20, 2018Fresno, CAFood/CosmeticsNo Action Indicated (NAI)3002994577
Oct 6, 2016Fresno, CAFood/CosmeticsVoluntary Action Indicated (VAI)3002994577
Apr 5, 2013Fresno, CAFood/CosmeticsOfficial Action Indicated (OAI)3002994577
Apr 5, 2012Fresno, CADrugsVoluntary Action Indicated (VAI)3002994577

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 3002994577Fresno, CA7Sep 3, 2024

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