# FDA Inspection 846350 - Quality Life Technologies Co. Ltd. - June 06, 2013

Source: https://www.keypedia.com/records/fda_inspections/quality-life-technologies-co-ltd/911b2615-443d-4752-be0e-1bc2846c583a
Source feed: FDA_Inspections

> FDA Inspection 846350 for Quality Life Technologies Co. Ltd. on June 06, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 846350
- Company Name: Quality Life Technologies Co. Ltd.
- Inspection Date: 2013-06-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1300520 - 2025-12-18](https://www.keypedia.com/records/fda_inspections/quality-life-technologies-co-ltd/b0be547e-922a-4196-b86a-01ecad4b23e8)
- [FDA Inspection 1300520 - 2025-12-18](https://www.keypedia.com/records/fda_inspections/quality-life-technologies-co-ltd/624b6403-df35-4dda-9507-b4dfef4a39e3)
- [FDA Inspection 1300520 - 2025-12-18](https://www.keypedia.com/records/fda_inspections/quality-life-technologies-co-ltd/a00f3764-01bf-4fd7-8f81-42c961058f32)

Company: https://www.keypedia.com/companies/quality-life-technologies-co-ltd/01f3d2f8-258b-4759-9ff9-8b53ba3dcd99

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