# FDA Inspection 1089069 - Clearpath Surgical, Inc. - March 20, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/clearpath-surgical-inc/0871edb9-5caf-4a18-8383-a950681564ac
Source feed: FDA_Inspections

> FDA Inspection 1089069 for Clearpath Surgical, Inc. on March 20, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1089069
- Company Name: Clearpath Surgical, Inc.
- Inspection Date: 2019-03-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1089069 - 2019-03-20](https://www.globalkeysolutions.net/records/fda_inspections/clearpath-surgical-inc/63447d44-6127-4bf4-85bb-44eef5d2b02c)

Company: https://www.globalkeysolutions.net/companies/clearpath-surgical-inc/977baddd-ee47-4567-8043-8bd0af6846b7

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7