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Prisma Health

FDA Regulatory Profile

Prisma Health has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 29, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections7Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 29, 2025Greenville, SCBiologicsNo Action Indicated (NAI)3000207045
Jun 22, 2023Greenville, SCBiologicsNo Action Indicated (NAI)3000207045
Apr 11, 2019Greenville, SCBiologicsNo Action Indicated (NAI)3000207045
Apr 13, 2017Greenville, SCBiologicsNo Action Indicated (NAI)3000207045
Jun 10, 2015Greenville, SCBiologicsNo Action Indicated (NAI)3000207045
Jan 30, 2013Greenville, SCBiologicsNo Action Indicated (NAI)3000207045
Nov 18, 2010Greenville, SCBiologicsVoluntary Action Indicated (VAI)3000207045

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 3000207045Greenville, SC7May 29, 2025

FDA data resources

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