FDA Inspection 969946 — Curonix LLC

Curonix LLC — FEI 3010676138

The FDA completed an inspection of Curonix LLC on Jan 29, 2016 in Pompano Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 29, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Pompano Beach, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
424921 CFR 821.25(c)Not established, maintained