Rapp Medical Systems, Inc.

FDA Regulatory Profile

Rapp Medical Systems, Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 1, 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
Inspections8Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 1, 2025Indianapolis, INBiologicsNo Action Indicated (NAI)3004213881
Jun 27, 2018Indianapolis, INBiologicsNo Action Indicated (NAI)3004213881
Sep 7, 2016Indianapolis, INBiologicsNo Action Indicated (NAI)3004213881
Jun 2, 2014Indianapolis, INBiologicsNo Action Indicated (NAI)3004213881
Sep 23, 2013La Porte, INBiologicsNo Action Indicated (NAI)3004129571
Sep 12, 2012Indianapolis, INBiologicsNo Action Indicated (NAI)3004213881
Nov 15, 2011La Porte, INBiologicsNo Action Indicated (NAI)3004129571
Feb 9, 2009La Porte, INBiologicsNo Action Indicated (NAI)3004129571

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 3004213881Indianapolis, IN5Jul 1, 2025
FEI 3004129571La Porte, IN3Sep 23, 2013

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