# FDA Inspection 591327 - Titan USA, LLC formerly Amstech - June 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/titan-usa-llc-formerly-amstech/a99a0800-023d-4aab-b640-9120c8a5f05e
Source feed: FDA_Inspections

> FDA Inspection 591327 for Titan USA, LLC formerly Amstech on June 23, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 591327
- Company Name: Titan USA, LLC formerly Amstech
- Inspection Date: 2009-06-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 805759 - 2012-10-30](https://www.keypedia.com/records/fda_inspections/titan-usa-llc-formerly-amstech/1eae94cf-886b-4725-a54e-05531eefc6e2)

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