# FDA Inspection 817627 - Dyna-Tek Industries - January 24, 2013

Source: https://www.keypedia.com/records/fda_inspections/dyna-tek-industries/2da1ab8a-59cd-48b8-82b5-1d98568c173e
Source feed: FDA_Inspections

> FDA Inspection 817627 for Dyna-Tek Industries on January 24, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 817627
- Company Name: Dyna-Tek Industries
- Inspection Date: 2013-01-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 636306 - 2010-01-06](https://www.keypedia.com/records/fda_inspections/dyna-tek-industries/3f36ff36-9c92-488c-8f8b-692d61687122)

Company: https://www.keypedia.com/companies/dyna-tek-industries/9b1d38ee-8e44-4cee-9706-826a10aeda6a

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