# FDA Inspection 1295018 - Kyongbo Pharmaceutical Co., Ltd. - November 11, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/kyongbo-pharmaceutical-co-ltd/c26675f6-c274-473d-bee0-2c61d912cb35
Source feed: FDA_Inspections

> FDA Inspection 1295018 for Kyongbo Pharmaceutical Co., Ltd. on November 11, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1295018
- Company Name: Kyongbo Pharmaceutical Co., Ltd.
- Inspection Date: 2025-11-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs

## Related Documents

- [FDA Inspection 1295018 - 2025-11-11](https://www.globalkeysolutions.net/records/fda_inspections/kyongbo-pharmaceutical-co-ltd/5ccde842-fa1b-48e6-a19e-bf02447ba280)
- [FDA Inspection 1112024 - 2019-12-06](https://www.globalkeysolutions.net/records/fda_inspections/kyongbo-pharmaceutical-co-ltd/e47f28ad-5913-414d-bd46-7adf78a3cffc)
- [FDA Inspection 1036989 - 2017-12-01](https://www.globalkeysolutions.net/records/fda_inspections/kyongbo-pharmaceutical-co-ltd/56e3c3e7-a77a-49a6-97b8-9515a55dc75c)
- [FDA Inspection 961652 - 2016-02-26](https://www.globalkeysolutions.net/records/fda_inspections/kyongbo-pharmaceutical-co-ltd/267f8277-b77b-4975-b270-250594f78986)
- [FDA Inspection 736571 - 2011-06-28](https://www.globalkeysolutions.net/records/fda_inspections/kyongbo-pharmaceutical-co-ltd/474fa8a3-d6f1-4e36-bde6-acd95e42761f)

Company: https://www.globalkeysolutions.net/companies/kyongbo-pharmaceutical-co-ltd/6b8fd90f-4fa3-4c7b-9ed6-a8a8f4b511da