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Facility profile

AVA, Inc.

Testing & analysis · Drug product manufacturing · Willowbrook, IL

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.

AnalysisActive pharmaceutical ingredient (API) manufactureLabelManufacturePackRelabelRepack
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
Official action indicated (OAI)

Oct 21, 2025 · The findings may warrant official FDA action.

Matched compliance actions
Warning Letter · May 2026

Within five years · review the action and follow-up.

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Shows

Registration status and a latest matched official 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 history4 inspection records

FDA inspection history

4 records, May 2013 – Oct 2025 · 0 NAI · 3 VAI · 1 OAI

DateClassProject areaCitationsFY
Oct 21, 2025OAIDrug Quality Assurance2026
Sep 29, 2021VAIDrug Quality AssuranceYes2021
Mar 30, 2016VAIDrug Quality Assurance2016
May 15, 2013VAIDrug Quality Assurance2013

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

Matched compliance actions

May 1, 2026Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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

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