# Curonix LLC – FDA Inspection, Feb 15, 2019

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

> FDA inspection 1079720 of Curonix LLC, February 15, 2019. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079720
- Company Name: Curonix LLC
- Inspection Date: 2019-02-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1223508 - 2023-11-08](https://www.keypedia.com/records/fda_inspections/curonix-llc/77b57c36-3ef7-4189-9331-aca2df7b6e24)
- FDA Inspection 1174085 - 2022-06-24
- FDA Inspection 969946 - 2016-01-29

## Related Officers

- [Investigator](https://www.keypedia.com/people/david-m-wilkinson/5e81ba03-7602-46d6-b675-26efc77d28db)
- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

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

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