# FDA Inspection 805759 - Titan USA, LLC formerly Amstech - October 30, 2012

Source: https://www.keypedia.com/records/fda_inspections/titan-usa-llc-formerly-amstech/1eae94cf-886b-4725-a54e-05531eefc6e2
Source feed: FDA_Inspections

> FDA Inspection 805759 for Titan USA, LLC formerly Amstech on October 30, 2012. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805759
- Company Name: Titan USA, LLC formerly Amstech
- Inspection Date: 2012-10-30
- Classification: Official Action Indicated (OAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 591327 - 2009-06-23](https://www.keypedia.com/records/fda_inspections/titan-usa-llc-formerly-amstech/a99a0800-023d-4aab-b640-9120c8a5f05e)

Company: https://www.keypedia.com/companies/titan-usa-llc-formerly-amstech/e36db6c0-9e6c-4c25-85af-20d478efdae0

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