Tokyo Chemical Industry Co., Ltd.
FDA Inspections Database

Tokyo Chemical Industry Co., Ltd.

FDA Inspections Database

U.S. FDA inspection classifications and citation records from the official FDA inspection database.

VAI · Voluntary Action Indicated Japan
  • Total Records 3
  • Latest Inspection 2025-05-16
  • Data Source U.S. FDA
  • Last Updated 2025-08-08
Company Overview

Company

Tokyo Chemical Industry Co., Ltd.

Country

Japan

Social Profiles

Company Snapshot

Tokyo Chemical Industry Co., Ltd.

4-10-2 Nihonbashi-honcho, Chuo-ku, Tokyo

Japan

www.tcichemicals.com globalbusiness@TCIchemicals.com View on Map
FDA Inspections Timeline (3 records)
2025
16 May
Voluntary Action Indicated VAI

Legal Name

Tokyo Chemical Industry Co., Ltd.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2025-05-16

FMD Date

2025-08-08

Fiscal Year

2025

State

Fukaya, Japan

Location

Fukaya, , Japan

Inspection Info

Fiscal Year: 2025
Citations: No

2018
19 Oct
Voluntary Action Indicated VAI

Legal Name

Tokyo Chemical Industry Co., Ltd.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2018-10-19

FMD Date

2018-11-27

Fiscal Year

2019

State

Fukaya, Japan

Location

Fukaya, , Japan

Inspection Info

Fiscal Year: 2019
Citations: No

2015
06 Feb
Voluntary Action Indicated VAI

Legal Name

Tokyo Chemical Industry Co., Ltd.

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2015-02-06

FMD Date

2015-04-17

Fiscal Year

2015

State

Fukaya, Japan

Location

Fukaya, , Japan

Inspection Info

Fiscal Year: 2015
Citations: No

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Classification Breakdown
3 total
  • VAI (Voluntary Action Indicated)
Official Source

All data is sourced from the official FDA inspection database maintained by the U.S. Food and Drug Administration.

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Record Details Preview

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Location

Fukaya, , Japan

Inspection Info

Fiscal Year: 2025
Citations: No

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FDA inspection data is compiled from publicly available U.S. FDA inspection classification records.

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