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Performance Orthopedics Associates

FDA Regulatory Profile

Performance Orthopedics Associates has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 13, 2025 · VAI

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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
Inspections4Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 13, 2025Mountain Brk, ALBiologicsVoluntary Action Indicated (VAI)3014678321
Feb 22, 2022Mountain Brk, ALBiologicsNo Action Indicated (NAI)3014678321
Nov 13, 2013Birmingham, ALDevicesNo Action Indicated (NAI)3007793285
Nov 19, 2009Birmingham, ALBiologicsNo Action Indicated (NAI)3007793285

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 3014678321Mountain Brk, AL2Jun 13, 2025
FEI 3007793285Birmingham, AL2Nov 13, 2013

FDA data resources

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