# FDA Inspection 574552 - Suretex, Ltd. - February 19, 2009

Source: https://www.keypedia.com/records/fda_inspections/suretex-ltd/29995168-5dc4-408d-bd02-7f89321c87a6
Source feed: FDA_Inspections

> FDA Inspection 574552 for Suretex, Ltd. on February 19, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 574552
- Company Name: Suretex, Ltd.
- Inspection Date: 2009-02-19
- 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 574552 - 2009-02-19](https://www.keypedia.com/records/fda_inspections/suretex-ltd/0ce907f9-5507-49d4-b678-2777c87b816e)

Company: https://www.keypedia.com/companies/suretex-ltd/1f1cd40d-4638-4158-bc0d-e69efc74429e

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