# FDA Inspection 1060765 - Surefire Medical Inc. - August 01, 2018

Source: https://www.keypedia.com/records/fda_inspections/surefire-medical-inc/c8d12449-6d90-419e-8eca-6d691719901b
Source feed: FDA_Inspections

> FDA Inspection 1060765 for Surefire Medical Inc. on August 01, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1060765
- Company Name: Surefire Medical Inc.
- Inspection Date: 2018-08-01
- 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 1060765 - 2018-08-01](https://www.keypedia.com/records/fda_inspections/surefire-medical-inc/8fcc1770-55fa-49db-850d-33ae47bace45)

Company: https://www.keypedia.com/companies/surefire-medical-inc/cca1819d-ab1c-4882-bef2-dd947163da0d

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