# FDA Inspection 708150 - Interlace Medical, Inc - July 09, 2010

Source: https://www.keypedia.com/records/fda_inspections/interlace-medical-inc/a500cb75-8353-4e08-9639-1bbbf2a4fe4d
Source feed: FDA_Inspections

> FDA Inspection 708150 for Interlace Medical, Inc on July 09, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 708150
- Company Name: Interlace Medical, Inc
- Inspection Date: 2010-07-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/interlace-medical-inc/8f27b568-0f4b-4442-ae80-fb2014971fc8

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