# FDA Inspection 788843 - Surefire Medical, Inc - June 22, 2012

Source: https://www.keypedia.com/records/fda_inspections/surefire-medical-inc/cd587c2a-78d1-4bcd-99d9-35c5ddf152e6
Source feed: FDA_Inspections

> FDA Inspection 788843 for Surefire Medical, Inc on June 22, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 788843
- Company Name: Surefire Medical, Inc
- Inspection Date: 2012-06-22
- 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 788843 - 2012-06-22](https://www.keypedia.com/records/fda_inspections/surefire-medical-inc/fc04ac35-9d13-42d2-b6ea-15a52bc8e7ee)

Company: https://www.keypedia.com/companies/surefire-medical-inc/318735fc-d9b7-47b7-b18d-ab45a9c94c94

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