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Facility profile

Baxter Healthcare Corporation

Testing & analysis · Drug product manufacturing · Marion, NC

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed15 registered company locations
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) manufactureLabelManufacturePackSterilize
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Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Official action indicated (OAI)

Feb 9, 2024 · The findings may warrant official FDA action.

Matched compliance actions
Past action on file · 2013

More than five years old · review later records.

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Shows

Registration status and a latest matched official action indicated inspection.

Doesn’t show

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Method and source details
View full inspection and compliance history16 inspection records

FDA inspection history

16 records, Aug 2009 – Feb 2024 · 4 NAI · 6 VAI · 6 OAI

DateClassProject areaCitationsFY
Feb 9, 2024OAIDrug Quality AssuranceYes2024
Oct 31, 2023OAIBlood and Blood ProductsYes2024
May 12, 2022NAIVaccines and Allergenic ProductsYes2022
May 12, 2022OAIBlood and Blood ProductsYes2022
Jul 1, 2021NAIDrug Quality Assurance2021
Nov 17, 2017VAIDrug Quality AssuranceYes2018
Feb 26, 2016OAIDrug Quality AssuranceYes2016
Jan 24, 2014VAIDrug Quality AssuranceYes2014
Nov 16, 2012OAIMonitoring of Marketed Animal Drugs, Feed, and DevicesYes2013
Nov 16, 2012OAIDrug Quality AssuranceYes2013
Aug 31, 2012VAIMonitoring of Marketed Animal Drugs, Feed, and DevicesYes2012
Aug 31, 2012VAICompliance: DevicesYes2012
Aug 31, 2012VAIDrug Quality AssuranceYes2012
Aug 27, 2010NAIDrug Quality Assurance2010
Aug 27, 2010NAICompliance: Devices2010
Aug 19, 2009VAIDrug Quality Assurance2009

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

Matched compliance actions

May 31, 2013Warning Letter · CDER
Unclaimed profile

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

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