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Dr. Joel Kaplan, Inc.

FDA Regulatory Profile

Dr. Joel Kaplan, Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
Jun 27, 2025 · NAI

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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
Inspections6Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 27, 2025San Diego, CADevicesNo Action Indicated (NAI)3001890611
Jun 30, 2023San Diego, CADevicesOfficial Action Indicated (OAI)3001890611
Dec 16, 2021San Diego, CAFood/CosmeticsNo Action Indicated (NAI)3001890611
Nov 1, 2017San Diego, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001890611
Dec 18, 2014San Diego, CADevicesVoluntary Action Indicated (VAI)3001890611
Jul 17, 2013San Diego, CADevicesOfficial Action Indicated (OAI)3001890611

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 3001890611San Diego, CA6Jun 27, 2025

FDA data resources

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