Enforcement record

Administrative Guidance disclosure naming 株式会社こころ

株式会社こころ (Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices)

This page records one action from a Japanese government disclosure, including the published name, governing law, authority, action details, and official source.

Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical DevicesMinistry of Health, Labour and WelfareGovernment disclosure28 July 2020

Action type

Administrative Guidance

Law

Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices

Authority

Ministry of Health, Labour and Welfare

Action date

28 July 2020

Current page: Enforcement record

This screen focuses on one disclosed action: the published name, governing law, authority, facts, source status, and review evidence.

Source verification

Public-source and preservation status

Publishing authority
Ministry of Health, Labour and Welfare
Official source URL
Recorded by RegBase
Entity match
Not confirmed; shown under the published name
Kiroku preservation
Queued for preservation
Captured: Jul 12, 2026, 03:34 PM JST

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Action summary

Company
株式会社こころJapanese only
Original: 株式会社こころ
Governing law
Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices
薬機法
Action type
Administrative Guidance
行政指導
Action date
28 July 2020
Issuing authority
Ministry of Health, Labour and Welfare
厚生労働省
Industry context
健康食品

Violation

Machine-translated summary — verify against original

Based on the submission of two types of CBD products, a total of eight products, the ingredients were analyzed. The analysis revealed that three units of CBD Oil Pro900 (10 mL capacity) and two units of CBD Oil Pro2700 (30 mL capacity) contained trace amounts of the cannabis component THC.

Show original Japanese text

同社が回収したCBD製品2種類8製品の提出を受け、成分の分析を行いました。分析の結果、CBDオイルPro900(容量10mL)3製品、CBDオイルPro2700(容量30mL)2製品から、微量の大麻成分THCが検出されました。

Compliance context

Low-medium

Administrative guidance or supervision was publicly disclosed by the authority.

Health product law covering pharmaceuticals, medical devices, cosmetics, quasi-drugs, labeling, and advertising.

Use as a monitoring signal. Confirm details before treating it as a formal sanction.

This context is an operational aid for review workflows, not a credit opinion or legal conclusion.

About this recordAggregated and translated from public Japanese government disclosures. The English text is for reference only — authoritative content is the linked Japanese source.