# FDA 483 - Daewoo Pharmaceutical Co., Ltd. - January 15, 2025

Source: https://www.keypedia.com/records/483/daewoo-pharmaceutical-co-ltd/8e464b2d-3dde-4fe4-b699-ac762e20ab1e

> FDA 483 for Daewoo Pharmaceutical Co., Ltd. on January 15, 2025. Product: Drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Daewoo Pharmaceutical Co., Ltd.
- Inspection Date: 2025-01-15
- Product Type: Drugs
- Office Name: Foreign - CDER (Non-Bioresearch Monitoring)
- Summary: I am sorry, but I cannot create a concise summary of the FDA 483 document as the actual content of the document was not provided. The input only contained a list of page numbers (Page 1 of 18 through Page 18 of 18) and not the text itself. To generate the summary, I would need the full text of the FDA 483 document, including details such as the company name, inspection dates, specific observations regarding violations or issues, the relevant regulatory framework, and any explicitly or implicitly required actions based on the findings. Please provide the document content so I can fulfill your request accurately and professionally.

## Related Documents

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- [WARNING_LETTER - 2025-01-15](https://www.keypedia.com/records/warning_letter/daewoo-pharmaceutical-co-ltd/b2da3b8e-d146-4e6e-9151-ac586707c077)

## Related Officers

- [Rowena S. Nguyen](https://www.keypedia.com/people/rowena-s-nguyen/ae39318e-1653-467c-94cc-26f8929441ac)
- [Drug National Expert](https://www.keypedia.com/people/sandra-a-boyd/c469103a-0917-407a-b9d1-98273358dfeb)

Company: https://www.keypedia.com/companies/daewoo-pharmaceutical-co-ltd/440e3629-5661-4fac-bc0e-71ae7f78f63b

Office: https://www.keypedia.com/offices/foreign-cder-non-bioresearch-monitoring/279f5818-f62e-40c9-951c-cfbc7f929fa1