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Parexel International (MA) Corporation

FDA Regulatory Profile

Parexel International (MA) Corporation has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Mar 5, 2026 · 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
Inspections4Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 5, 2026Auburndale, MADrugsNo Action Indicated (NAI)3001812586
Dec 9, 2025Auburndale, MADrugsNo Action Indicated (NAI)3001812586
Nov 9, 2022Auburndale, MADrugsNo Action Indicated (NAI)3001812586
Feb 18, 2010Auburndale, MADevicesNo Action Indicated (NAI)3001812586

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 3001812586Auburndale, MA4Mar 5, 2026

FDA data resources

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