Labverity
Facility profile

Intertek USA Inc

Testing-focused facility · Whitehouse, NJ

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.

Analysis
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
No action indicated (NAI)

Sep 25, 2025 · No conditions warranted FDA action in this inspection.

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 no 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 history6 inspection records

FDA inspection history

6 records, Mar 2010 – Sep 2025 · 5 NAI · 1 VAI · 0 OAI

DateClassProject areaCitationsFY
Sep 25, 2025NAIDrug Quality Assurance2025
Mar 7, 2025VAIHuman Cellular, Tissue, and Gene TherapiesYes2025
Dec 21, 2020NAIDrug Quality Assurance2021
Aug 12, 2016NAIDrug Quality Assurance2016
Jan 21, 2013NAIDrug Quality Assurance2013
Mar 3, 2010NAIDrug 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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