# FDA Inspection 804875 - GRANTECH CO., LTD. - October 18, 2012

Source: https://www.keypedia.com/records/fda_inspections/grantech-co-ltd/e34ae79d-66f8-4d3d-a807-b783b752ed97
Source feed: FDA_Inspections

> FDA Inspection 804875 for GRANTECH CO., LTD. on October 18, 2012. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 804875
- Company Name: GRANTECH CO., LTD.
- Inspection Date: 2012-10-18
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 804875 - 2012-10-18](https://www.keypedia.com/records/fda_inspections/grantech-co-ltd/e31d7e2d-b509-408a-8b92-03f117c34fe7)

Company: https://www.keypedia.com/companies/grantech-co-ltd/e1bac3af-1143-488c-90ee-10671e19b2b3

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