# FDA Inspection 846616 - Durden Enterprises, LTD. - August 22, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/durden-enterprises-ltd/f76ed5d0-fc03-494e-8712-556ffe037ada/
Source feed: FDA_Inspections

> FDA Inspection 846616 for Durden Enterprises, LTD. on August 22, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 846616
- Company Name: Durden Enterprises, LTD.
- Inspection Date: 2013-08-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 846616 - 2013-08-22](https://www.globalkeysolutions.net/api/records/fda_inspections/durden-enterprises-ltd/820e6901-8028-4b95-8aad-6b3113e10594/)
- [FDA Inspection 620117 - 2009-09-15](https://www.globalkeysolutions.net/api/records/fda_inspections/durden-enterprises-ltd/8ac3d8a5-9aec-49eb-9edc-c3f159a6a157/)
- [FDA Inspection 620117 - 2009-09-15](https://www.globalkeysolutions.net/api/records/fda_inspections/durden-enterprises-ltd/524d1f44-741a-4f10-8768-182801b83134/)

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

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