# FDA Inspection 1091675 - Medicore Co., Ltd. - April 25, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/medicore-co-ltd/41f13bc3-837e-407b-942d-b0d880f74be5/
Source feed: FDA_Inspections

> FDA Inspection 1091675 for Medicore Co., Ltd. on April 25, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091675
- Company Name: Medicore Co., Ltd.
- Inspection Date: 2019-04-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1091675 - 2019-04-25](https://www.globalkeysolutions.net/api/records/fda_inspections/medicore-co-ltd/ff85238d-7b0d-4c4f-80ff-d6563ef3391d/)

Company: https://www.globalkeysolutions.net/companies/medicore-co-ltd/00ebb45b-0f71-4cd5-8215-bdf3dbdfbfa8

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