# Catheter Robotics, Incorporated - Inspection Records

Source: https://www.keypedia.com/companies/catheter-robotics-incorporated/fb1980ae-c222-4404-a0e4-7428edc68b3f

> Inspection records and compliance data for Catheter Robotics, Incorporated in Fort Mill, South Carolina. Access full analysis and detailed observations.

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## Details

- Name: Catheter Robotics, Incorporated
- FEI Number: 3010728615
- City: Fort Mill
- State: South Carolina
- Country Name: United States
- Address Line 1: 1670 Highway 160 W Ste 205
- Zip Code: 29708

## Related Documents

- [483 - Catheter Robotics, Incorporated - 2025-07-02](https://www.keypedia.com/records/483/catheter-robotics-incorporated/ecaa6c93-c308-498f-9121-3840932aaf3a) — source: FDA, date: July 2, 2025
- [FDA Inspection 1274502 - Catheter Robotics, Incorporated - 2025-07-02](https://www.keypedia.com/records/fda_inspections/catheter-robotics-incorporated/7320c0cd-10e9-4af2-9887-8b990060d8b2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2025
- [FDA Inspection 1274502 - Catheter Robotics, Incorporated - 2025-07-02](https://www.keypedia.com/records/fda_inspections/catheter-robotics-incorporated/7aa03f20-eedc-490c-8e84-6bf2a89198d4) — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2025
- [FDA Inspection 1274502 - Catheter Robotics, Incorporated - 2025-07-02](https://www.keypedia.com/records/fda_inspections/catheter-robotics-incorporated/f87eae92-268e-43b0-bd8b-b65c6a18e845) — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2025
- [FDA Inspection 1274502 - Catheter Robotics, Incorporated - 2025-07-02](https://www.keypedia.com/records/fda_inspections/catheter-robotics-incorporated/1d937629-2c72-4595-a195-ae3ec3846157) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2025
- [FDA Inspection 1106129 - Catheter Robotics, Incorporated - 2019-07-24](https://www.keypedia.com/records/fda_inspections/catheter-robotics-incorporated/c5a23119-e1a5-4a28-b0d6-9c1f9a4ff598) — classification: No Action Indicated (NAI), source: FDA, date: July 24, 2019

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