OCPP LLC

FDA Regulatory Profile

OCPP LLC has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Feb 25, 2026 · 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
Inspections7Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 25, 2026Corona, CAVeterinaryVoluntary Action Indicated (VAI)3011530695
Feb 10, 2025Corona, CAVeterinaryVoluntary Action Indicated (VAI)3011530695
Apr 6, 2023Corona, CAVeterinaryVoluntary Action Indicated (VAI)3011530695
May 26, 2021Corona, CAVeterinaryOfficial Action Indicated (OAI)3011530695
Sep 4, 2019Corona, CAVeterinaryVoluntary Action Indicated (VAI)3011530695
May 15, 2018Corona, CAVeterinaryNo Action Indicated (NAI)3011530695
Apr 24, 2017Corona, CAFood/CosmeticsNo Action Indicated (NAI)3011530695

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 3011530695Corona, CA7Feb 25, 2026

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