# FDA Inspection 1230811 - Guangdong Welland Technology Co.,Ltd. - January 25, 2024

Source: https://www.keypedia.com/records/fda_inspections/guangdong-welland-technology-coltd/090bd677-08f3-4a08-8272-c88e407293ef
Source feed: FDA_Inspections

> FDA Inspection 1230811 for Guangdong Welland Technology Co.,Ltd. on January 25, 2024. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1230811
- Company Name: Guangdong Welland Technology Co.,Ltd.
- Inspection Date: 2024-01-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1230811 - 2024-01-25](https://www.keypedia.com/records/fda_inspections/guangdong-welland-technology-coltd/89f705ac-b61c-4cf9-8c04-30233692a71f)
- [FDA Inspection 1111038 - 2019-10-31](https://www.keypedia.com/records/fda_inspections/guangdong-welland-technology-coltd/03a9912b-1ff6-4f9a-a493-1df7ac2aded6)
- [FDA Inspection 1111038 - 2019-10-31](https://www.keypedia.com/records/fda_inspections/guangdong-welland-technology-coltd/7fca74b1-9b1c-4304-bfc2-15dff1d25e7b)

Company: https://www.keypedia.com/companies/guangdong-welland-technology-coltd/402584b0-b784-4fac-a601-410379431b0a

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