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Facility profile

Catalent Greenville, Inc.

Testing & analysis · Drug product manufacturing · Greenville, NC

FDA recordFDA directory updated Jul 22, 2026Profile not yet claimed23 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.

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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 22, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Oct 24, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

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

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Method and source details
View full inspection and compliance history13 inspection records

FDA inspection history

13 records, Nov 2009 – Oct 2025 · 7 NAI · 6 VAI · 0 OAI

DateClassProject areaCitationsFY
Oct 24, 2025VAIDrug Quality AssuranceYes2026
Jan 31, 2024NAIDrug Quality Assurance2024
Jul 12, 2019VAIDrug Quality AssuranceYes2019
Aug 24, 2018NAIBioresearch Monitoring2018
Apr 13, 2017NAIDrug Quality Assurance2017
Jul 14, 2016NAIDrug Quality Assurance2016
May 2, 2014NAIDrug Quality Assurance2014
Aug 21, 2013NAIBioresearch Monitoring2013
May 11, 2012VAIDrug Quality Assurance2012
May 11, 2012VAIDrug Quality AssuranceYes2012
Mar 18, 2011VAIDrug Quality Assurance2011
Oct 1, 2010VAIDrug Quality Assurance2011
Nov 13, 2009NAIDrug Quality Assurance2010

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

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

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

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