# Defibtech, LLC – FDA Inspection, Feb 8, 2011

Source: https://www.keypedia.com/records/fda_inspections/defibtech-llc/1483d6b5-3b1f-452c-9aec-9256e9c56b43
Source feed: FDA_Inspections

> FDA inspection 708589 of Defibtech, LLC, February 08, 2011. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 708589
- Company Name: Defibtech, LLC
- Inspection Date: 2011-02-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1024269 - 2017-08-16
- FDA Inspection 876495 - 2014-04-25
- FDA Inspection 760057 - 2011-12-21
- [FDA Inspection 675878 - 2010-08-18](https://www.keypedia.com/records/fda_inspections/defibtech-llc/81857c49-3f12-445f-916c-639724f733b1)

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