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Facility profile

International Medication Systems, Ltd.

Testing & analysis · Drug product manufacturing · South El Monte, CA

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

AnalysisActive pharmaceutical ingredient (API) manufactureDistributeLabelManufacturePack
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Official action indicated (OAI)

Dec 19, 2025 · The findings may warrant official FDA action.

Matched compliance actions
Warning Letter · Jul 2026

Within five years · review the action and follow-up.

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Shows

Registration status and a latest matched official action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Review the underlying findings, response, and subsequent follow-up before qualification.

Method and source details
View full inspection and compliance history18 inspection records

FDA inspection history

18 records, Nov 2008 – Dec 2025 · 6 NAI · 11 VAI · 1 OAI

DateClassProject areaCitationsFY
Dec 19, 2025OAIDrug Quality AssuranceYes2026
Oct 2, 2024NAIBioresearch Monitoring2025
May 25, 2022VAIDrug Quality AssuranceYes2022
Jul 16, 2021NAIDrug Quality Assurance2021
Dec 20, 2019NAIDrug Quality Assurance2020
Feb 9, 2017VAICompliance: Devices2017
Feb 9, 2017VAIDrug Quality Assurance2017
Dec 7, 2016VAIDrug Quality Assurance2017
Dec 7, 2016NAICompliance: Devices2017
Aug 10, 2015VAIDrug Quality Assurance2015
Aug 10, 2015VAICompliance: Devices2015
Sep 12, 2014VAIDrug Quality AssuranceYes2014
Jul 24, 2013NAIDrug Quality Assurance2013
Jun 17, 2013VAIDrug Quality Assurance2013
Aug 31, 2012VAIDrug Quality Assurance2012
Jun 15, 2011NAIDrug Quality Assurance2011
Aug 31, 2009VAIDrug Quality Assurance2009
Nov 24, 2008VAIDrug Quality Assurance2009

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

Jul 2, 2026Warning Letter · CDER
Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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