FDA Inspection 1223508 — Curonix LLC

Curonix LLC — FEI 3010676138

The FDA completed an inspection of Curonix LLC on Nov 8, 2023 in Pompano Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 8, 2023
Fiscal Year
2024
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
311721 CFR 820.70(i)Software validation for automated processes
313021 CFR 820.100(a)Lack of or inadequate procedures
328621 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate