# FDA Inspection 570521 - Tegra Medical, LLC - March 18, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/tegra-medical-llc/53105e19-3e14-4c0a-a705-efe1dc915361
Source feed: FDA_Inspections

> FDA Inspection 570521 for Tegra Medical, LLC on March 18, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 570521
- Company Name: Tegra Medical, LLC
- Inspection Date: 2009-03-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 768849 - 2012-01-20](https://www.globalkeysolutions.net/records/fda_inspections/tegra-medical-llc/dccd3503-09c2-4c1d-abc2-48b8781f35a7)
- [FDA Inspection 570521 - 2009-03-18](https://www.globalkeysolutions.net/records/fda_inspections/tegra-medical-llc/2f9533bf-9bc2-4d61-969e-afb8286b7ad0)

Company: https://www.globalkeysolutions.net/companies/tegra-medical-llc/331230af-e141-44a2-bac3-74d96f878889

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