# FDA Inspection 1060124 - Nuga Medical Co., Ltd. - July 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/nuga-medical-co-ltd/20c3dfc8-3cca-4792-8a15-b54d81f01461
Source feed: FDA_Inspections

> FDA Inspection 1060124 for Nuga Medical Co., Ltd. on July 27, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1060124
- Company Name: Nuga Medical Co., Ltd.
- Inspection Date: 2018-07-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1194084 - 2022-12-08](https://www.keypedia.com/records/fda_inspections/nuga-medical-co-ltd/fa36f64b-bbf1-4030-b416-4ca8e0a672b6)
- [FDA Inspection 1194084 - 2022-12-08](https://www.keypedia.com/records/fda_inspections/nuga-medical-co-ltd/15970d93-4b31-4887-9b71-8595632daf78)
- [FDA Inspection 898365 - 2014-08-28](https://www.keypedia.com/records/fda_inspections/nuga-medical-co-ltd/2dd22b49-0027-4ac5-8a85-edbd06a76a29)

Company: https://www.keypedia.com/companies/nuga-medical-co-ltd/0cf1dd61-d88d-4cfe-b1fb-447cd38d59bc

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