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Kobo Products, Inc.

Active pharmaceutical ingredient (API) manufacturing · South Plainfield, 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.

Active pharmaceutical ingredient (API) manufacture
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)

May 9, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

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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 history10 inspection records

FDA inspection history

10 records, Sep 2010 – May 2025 · 1 NAI · 9 VAI · 0 OAI

DateClassProject areaCitationsFY
May 9, 2025VAIDrug Quality Assurance2025
Aug 18, 2020VAIDrug Quality Assurance2020
Mar 13, 2015VAIDrug Quality Assurance2015
Mar 13, 2015VAIDrug Quality Assurance2015
Mar 13, 2015VAIDrug Quality Assurance2015
Dec 16, 2013VAIDrug Quality Assurance2014
Nov 28, 2011NAIDrug Quality Assurance2012
Sep 30, 2010VAIDrug Quality Assurance2010
Sep 30, 2010VAIDrug Quality Assurance2010
Sep 30, 2010VAIDrug 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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