# Durden Enterprises, LTD. – FDA Inspection, Sep 15, 2009

Source: https://www.keypedia.com/records/fda_inspections/durden-enterprises-ltd/8ac3d8a5-9aec-49eb-9edc-c3f159a6a157
Source feed: FDA_Inspections

> FDA inspection 620117 of Durden Enterprises, LTD., September 15, 2009. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 620117
- Company Name: Durden Enterprises, LTD.
- Inspection Date: 2009-09-15
- 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: 4

## Related Documents

- FDA Inspection 846616 - 2013-08-22

Company: https://www.keypedia.com/companies/durden-enterprises-ltd/2bfa9655-3175-4bd0-8545-1646c85feaec

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