# FDA Inspection 802345 - ASO LLC - October 05, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/aso-llc/d37d8c6d-fe20-477a-91fd-d0a63fa37745
Source feed: FDA_Inspections

> FDA Inspection 802345 for ASO LLC on October 05, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 802345
- Company Name: ASO LLC
- Inspection Date: 2012-10-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1067557 - 2018-09-12](https://www.globalkeysolutions.net/records/fda_inspections/aso-llc/aced49db-8b25-4db8-b9a2-514f70167863)
- [FDA Inspection 802345 - 2012-10-05](https://www.globalkeysolutions.net/records/fda_inspections/aso-llc/6bc797da-f2ed-4fcb-859b-71821d20bbdb)

Company: https://www.globalkeysolutions.net/companies/aso-llc/7b0b2701-262b-480f-bece-142fa3b1a1f8

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