# FDA Inspection 956220 - Oishi Koseido Co., Ltd. - January 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/oishi-koseido-co-ltd/02961efe-e59f-46e7-8d55-25d786a0dcdd
Source feed: FDA_Inspections

> FDA Inspection 956220 for Oishi Koseido Co., Ltd. on January 29, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 956220
- Company Name: Oishi Koseido Co., Ltd.
- Inspection Date: 2016-01-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Company: https://www.keypedia.com/companies/oishi-koseido-co-ltd/07ae7f38-2728-4248-8ef1-ff0abd9a79e7

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