# FDA Inspection 593436 - Xitron Technologies Inc - July 10, 2009

Source: https://www.keypedia.com/records/fda_inspections/xitron-technologies-inc/8846688d-4797-4095-957b-6f7907106fff
Source feed: FDA_Inspections

> FDA Inspection 593436 for Xitron Technologies Inc on July 10, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 593436
- Company Name: Xitron Technologies Inc
- Inspection Date: 2009-07-10
- 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 593436 - 2009-07-10](https://www.keypedia.com/records/fda_inspections/xitron-technologies-inc/731a8d27-eca7-44cc-8415-b2a375d344b9)

Company: https://www.keypedia.com/companies/xitron-technologies-inc/eb3aefc1-3769-4569-a9cf-3c7b3ced6a07

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