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Facility profile

Cetylite Industries, Inc.

Testing & analysis · Drug product manufacturing · Pennsauken, NJ

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
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Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

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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)

Apr 7, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
Warning Letter · Apr 2022

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

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Shows

Registration status and a latest matched voluntary 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 history13 inspection records

FDA inspection history

13 records, Oct 2008 – Apr 2025 · 3 NAI · 8 VAI · 2 OAI

DateClassProject areaCitationsFY
Apr 7, 2025VAICompliance: DevicesYes2025
Apr 7, 2025NAIPostmarket Assurance: DevicesYes2025
Dec 9, 2024VAIDrug Quality AssuranceYes2025
Mar 2, 2023OAIDrug Quality AssuranceYes2023
Sep 24, 2021OAIDrug Quality AssuranceYes2021
May 29, 2018VAIBioresearch MonitoringYes2018
May 29, 2018VAIDrug Quality AssuranceYes2018
Nov 19, 2015VAIDrug Quality AssuranceYes2016
Jul 12, 2013VAIDrug Quality Assurance2013
Jul 12, 2013NAICompliance: Devices2013
Apr 26, 2011VAICompliance: DevicesYes2011
Apr 26, 2011VAIDrug Quality AssuranceYes2011
Oct 14, 2008NAIDrug Quality Assurance2009

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

Matched compliance actions

Apr 13, 2022Warning Letter · CDER
Unclaimed profile

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

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