# FDA Inspection 1079720 - Curonix LLC - February 15, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/curonix-llc/d9f87d57-c2f2-47f2-a623-55ae4fdc0e0d
Source feed: FDA_Inspections

> FDA Inspection 1079720 for Curonix LLC on February 15, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1079720
- Company Name: Curonix LLC
- Inspection Date: 2019-02-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1223508 - 2023-11-08](https://www.globalkeysolutions.net/records/fda_inspections/curonix-llc/51531aa8-bbd8-4c39-bbc3-ca3cf346b572)
- [FDA Inspection 1223508 - 2023-11-08](https://www.globalkeysolutions.net/records/fda_inspections/curonix-llc/77b57c36-3ef7-4189-9331-aca2df7b6e24)
- [FDA Inspection 1174085 - 2022-06-24](https://www.globalkeysolutions.net/records/fda_inspections/curonix-llc/81bbd38f-32a3-4960-b0f3-7a3de9a03dc4)
- [FDA Inspection 1174085 - 2022-06-24](https://www.globalkeysolutions.net/records/fda_inspections/curonix-llc/ab08bca0-9549-408e-a0e0-4ed2d09b199a)
- [FDA Inspection 969946 - 2016-01-29](https://www.globalkeysolutions.net/records/fda_inspections/curonix-llc/fadd13ce-58b3-4e52-ac03-a3e65b0f02a4)

Company: https://www.globalkeysolutions.net/companies/curonix-llc/2840a5e9-814d-410e-a50b-656a3e56e1bd

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