# FDA Inspection 1037550 - Oishi Koseido Co Ltd - December 06, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/oishi-koseido-co-ltd/000ceccc-a243-4cf7-a957-89e2a1197286
Source feed: FDA_Inspections

> FDA Inspection 1037550 for Oishi Koseido Co Ltd on December 06, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037550
- Company Name: Oishi Koseido Co Ltd
- Inspection Date: 2017-12-06
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

Company: https://www.globalkeysolutions.net/companies/oishi-koseido-co-ltd/0da6cc2f-20e6-45a1-b0f6-d25ca34aecc1

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