Labverity
Facility profile

A.P. Deauville, LLC

Drug product manufacturing · Easton, PA

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.

LabelManufacture
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)

Jan 23, 2025 · The findings may warrant official FDA action.

Matched compliance actions
Past action on file · 2019

More than five years old · review later records.

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Shows

Registration status and a latest matched official action indicated inspection.

Doesn’t show

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Method and source details
View full inspection and compliance history8 inspection records

FDA inspection history

8 records, Apr 2011 – Jan 2025 · 0 NAI · 5 VAI · 3 OAI

DateClassProject areaCitationsFY
Jan 23, 2025OAIDrug Quality AssuranceYes2025
Aug 25, 2022OAIDrug Quality AssuranceYes2022
May 2, 2019OAIDrug Quality AssuranceYes2019
Sep 19, 2017VAIDrug Quality AssuranceYes2017
Feb 1, 2016VAIDrug Quality AssuranceYes2016
Mar 4, 2013VAIColors and Cosmetics TechnologyYes2013
Mar 4, 2013VAIDrug Quality AssuranceYes2013
Apr 21, 2011VAIDrug Quality AssuranceYes2011

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

Matched compliance actions

Nov 8, 2019Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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