Pharmaron Manufacturing Services (US) LLC

FDA Regulatory Profile

Pharmaron Manufacturing Services (US) LLC has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 17, 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 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 17, 2025Coventry, RIDrugsNo Action Indicated (NAI)1211201
Jan 23, 2020Coventry, RIDrugsVoluntary Action Indicated (VAI)1211201
Jul 27, 2016Coventry, RIDrugsVoluntary Action Indicated (VAI)1211201
Aug 15, 2014Coventry, RIDrugsVoluntary Action Indicated (VAI)1211201
Mar 21, 2012Coventry, RIDrugsVoluntary Action Indicated (VAI)1211201
May 5, 2010Coventry, RIDrugsVoluntary Action Indicated (VAI)1211201

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 1211201Coventry, RI6Jul 17, 2025

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