FDA inspection

Catheter Precision Inc.: FDA inspection ending Jul 2, 2025

FDA inspection 1274502 · Voluntary Action Indicated (VAI) · Fort Mill, SC

Key facts

Inspection ID 1274502
Firm Catheter Precision Inc.
FEI number 3010728615
Address 1670 Highway 160 W Ste 205
City Fort Mill
State SC
ZIP 29708
Country United States
Fiscal year 2025
Inspection end date Jul 2, 2025
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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