FDA Inspection 1106129 — Catheter Precision Inc.

Catheter Precision Inc. — FEI 3010728615

The FDA completed an inspection of Catheter Precision Inc. on Jul 24, 2019 in Fort Mill, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 24, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Fort Mill, SC (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.