Labverity
Facility profile

Pure Source, LLC

Drug product manufacturing · Packaging & labeling · Doral, FL

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.

LabelManufacturePackRepack
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
Voluntary action indicated (VAI)

Aug 31, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2019

More than five years old · review later records.

Understand this record

Use the evidence, then ask for fit.

Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

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

Ask next

Ask what was corrected and review any later inspection or follow-up record.

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

FDA inspection history

16 records, Sep 2009 – Aug 2023 · 0 NAI · 14 VAI · 2 OAI

DateClassProject areaCitationsFY
Aug 31, 2023VAIPostmarket Assurance: DevicesYes2023
Aug 31, 2023VAICompliance: DevicesYes2023
Aug 14, 2019VAIDrug Quality AssuranceYes2019
Mar 1, 2018OAIMonitoring of Marketed Animal Drugs, Feed, and DevicesYes2018
Mar 1, 2018OAIDrug Quality AssuranceYes2018
Jun 23, 2017VAIFood Composition, Standards, Labeling and EconYes2017
Feb 24, 2014VAIDrug Quality AssuranceYes2014
Feb 24, 2014VAIMonitoring of Marketed Animal Drugs, Feed, and DevicesYes2014
Sep 22, 2011VAIFood Composition, Standards, Labeling and EconYes2011
Sep 22, 2011VAIMonitoring of Marketed Animal Drugs, Feed, and DevicesYes2011
Sep 22, 2011VAIColors and Cosmetics TechnologyYes2011
Sep 22, 2011VAIUnapproved and Misbranded DrugsYes2011
Sep 22, 2011VAIDrug Quality AssuranceYes2011
Sep 29, 2009VAIUnapproved and Misbranded DrugsYes2009
Sep 29, 2009VAIColors and Cosmetics TechnologyYes2009
Sep 29, 2009VAIDrug Quality AssuranceYes2009

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

Matched compliance actions

Feb 20, 2019Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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

Ask about services