# FDA Inspection 1031995 - Kolmar Korea Co., Ltd. - Gwanjeong Factory - September 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/kolmar-korea-co-ltd-gwanjeong-factory/6ee2d17f-971f-4c7c-8d3b-5606f135ab22
Source feed: FDA_Inspections

> FDA Inspection 1031995 for Kolmar Korea Co., Ltd. - Gwanjeong Factory on September 15, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031995
- Company Name: Kolmar Korea Co., Ltd. - Gwanjeong Factory
- Inspection Date: 2017-09-15
- 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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Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c