# FDA Inspection 940792 - Defibtech, LLC - August 27, 2015

Source: https://www.keypedia.com/records/fda_inspections/defibtech-llc/571eac66-db05-4e2d-af70-f7fee5d66812
Source feed: FDA_Inspections

> FDA Inspection 940792 for Defibtech, LLC on August 27, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 940792
- Company Name: Defibtech, LLC
- Inspection Date: 2015-08-27
- 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 793745 - 2012-08-08](https://www.keypedia.com/records/fda_inspections/defibtech-llc/bf5a64a3-7c8c-446a-b03c-b28f75738f65)
- [FDA Inspection 675880 - 2010-08-10](https://www.keypedia.com/records/fda_inspections/defibtech-llc/35f8d6ca-6c22-429c-a7dc-a9ae739af288)

Company: https://www.keypedia.com/companies/defibtech-llc/1faa7dd6-d6a1-4976-9414-1f19bdddb478

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