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Facility profile

Ajinomoto Company, Inc.

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Kanagawa 210-8680 · Japan

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed9 registered company locations
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) manufactureLabelRelabel
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
Voluntary action indicated (VAI)

Feb 21, 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 history6 inspection records

FDA inspection history

6 records, May 2009 – Feb 2025 · 3 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Feb 21, 2025VAIDrug Quality Assurance2025
Nov 8, 2019NAIDrug Quality Assurance2020
Sep 22, 2017NAIDrug Quality Assurance2017
Mar 13, 2015NAIDrug Quality Assurance2015
Sep 13, 2012VAIDrug Quality Assurance2012
May 29, 2009VAIDrug Quality Assurance2009

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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