# Surefire Medical Inc. – FDA Inspection, Aug 1, 2018

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

> FDA inspection 1060765 of Surefire Medical Inc., August 01, 2018. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1060765
- Company Name: Surefire Medical Inc.
- Inspection Date: 2018-08-01
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/vicky-l-cruz/282da571-56be-48f4-96c6-d590829b12c2)

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