# FDA Inspection 1020787 - Daito Kasei Kogyo Co., Ltd. - July 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/daito-kasei-kogyo-co-ltd/8c9a010c-9eee-4549-8889-0f555dda1ab8
Source feed: FDA_Inspections

> FDA Inspection 1020787 for Daito Kasei Kogyo Co., Ltd. on July 21, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020787
- Company Name: Daito Kasei Kogyo Co., Ltd.
- Inspection Date: 2017-07-21
- Classification: Official Action Indicated (OAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

Company: https://www.keypedia.com/companies/daito-kasei-kogyo-co-ltd/82e3b999-b9b9-4c78-b3f6-92b0cf5498ba

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c