Labverity
Facility profile

WES PHARMA INC

Testing & analysis · Drug product manufacturing · WESTMINSTER, MD

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.

AnalysisLabelManufacturePack
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)

Nov 20, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2009

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 history7 inspection records

FDA inspection history

7 records, Dec 2018 – Nov 2025 · 3 NAI · 4 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 20, 2025VAIDrug Quality AssuranceYes2026
Nov 21, 2023VAIDrug Quality AssuranceYes2024
Feb 18, 2022NAIDrug Quality Assurance2022
Apr 28, 2021NAIBioresearch Monitoring2021
Dec 20, 2019VAIDrug Quality Assurance2020
Apr 19, 2019NAIBioresearch Monitoring2019
Dec 13, 2018VAIDrug Quality Assurance2019

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

Matched compliance actions

Apr 9, 2009Injunction · CDER
Unclaimed profile

Service details not yet provided

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

Ask about services