# FDA Inspection 1024231 - Defibtech, LLC - August 16, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/defibtech-llc/56a79898-db85-41bd-a509-14bf67ac81b9
Source feed: FDA_Inspections

> FDA Inspection 1024231 for Defibtech, LLC on August 16, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024231
- Company Name: Defibtech, LLC
- Inspection Date: 2017-08-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/defibtech-llc/4ebf10b2-dd7d-449a-979b-c65820d96663

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