# FDA Inspection 675880 - Defibtech, LLC - August 10, 2010

Source: https://www.keypedia.com/records/fda_inspections/defibtech-llc/35f8d6ca-6c22-429c-a7dc-a9ae739af288
Source feed: FDA_Inspections

> FDA Inspection 675880 for Defibtech, LLC on August 10, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675880
- Company Name: Defibtech, LLC
- Inspection Date: 2010-08-10
- 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/1faa7dd6-d6a1-4976-9414-1f19bdddb478

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