# FDA Inspection 760057 - Defibtech, LLC - December 21, 2011

Source: https://www.keypedia.com/records/fda_inspections/defibtech-llc/690787c3-8a63-4a4d-811f-4e53afd61cfa
Source feed: FDA_Inspections

> FDA Inspection 760057 for Defibtech, LLC on December 21, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 760057
- Company Name: Defibtech, LLC
- Inspection Date: 2011-12-21
- 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.keypedia.com/companies/defibtech-llc/2d1df48a-49ee-431d-8535-840d912c1f36

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