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Facility profile

GCP Laboratories

Testing & analysis · Drug product manufacturing · Gulfport, MS

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
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Listed operations

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

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Due diligence

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
Voluntary action indicated (VAI)

May 13, 2022 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2009

More than five years old · review later records.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

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Method and source details
View full inspection and compliance history11 inspection records

FDA inspection history

11 records, Nov 2008 – May 2022 · 6 NAI · 3 VAI · 2 OAI

DateClassProject areaCitationsFY
May 13, 2022VAIDrug Quality AssuranceYes2022
Aug 7, 2019NAIFood Composition, Standards, Labeling and Econ2019
Jan 10, 2018NAIFood Composition, Standards, Labeling and Econ2018
Feb 4, 2015NAIFood Composition, Standards, Labeling and Econ2015
Feb 4, 2015NAIDrug Quality Assurance2015
Nov 4, 2011NAIFood Composition, Standards, Labeling and Econ2012
Nov 4, 2011NAIDrug Quality Assurance2012
Dec 9, 2009VAIDrug Quality AssuranceYes2010
Feb 19, 2009OAIDrug Quality AssuranceYes2009
Feb 19, 2009OAIUnapproved and Misbranded DrugsYes2009
Nov 6, 2008VAIDrug Quality AssuranceYes2009

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

Matched compliance actions

Aug 21, 2009Warning Letter · CDER
Unclaimed profile

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

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