# FDA Inspection 1287038 - KAIGEN PHARMA CO.,LTD. - September 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/kaigen-pharma-coltd/c563f8e7-3eb4-4dfc-bc1e-25ae92594062
Source feed: FDA_Inspections

> FDA Inspection 1287038 for KAIGEN PHARMA CO.,LTD. on September 26, 2025. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1287038
- Company Name: KAIGEN PHARMA CO.,LTD.
- Inspection Date: 2025-09-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1287038 - 2025-09-26](https://www.keypedia.com/records/fda_inspections/kaigen-pharma-coltd/350e0c6b-03f5-4a0e-a011-cb2842ff6d74)

Company: https://www.keypedia.com/companies/kaigen-pharma-coltd/3de7485c-9df0-4b98-bcd8-52341ed30431

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7