# FDA Inspection 639478 - Immucor GTI Diagnostics, Inc - January 13, 2010

Source: https://www.keypedia.com/records/fda_inspections/immucor-gti-diagnostics-inc/97a94f54-cdcc-4320-959c-b8645a3f5b01
Source feed: FDA_Inspections

> FDA Inspection 639478 for Immucor GTI Diagnostics, Inc on January 13, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 639478
- Company Name: Immucor GTI Diagnostics, Inc
- Inspection Date: 2010-01-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 977541 - 2016-02-01](https://www.keypedia.com/records/fda_inspections/immucor-gti-diagnostics-inc/b833029c-14ba-48a2-8423-5457049b218b)
- [FDA Inspection 977541 - 2016-02-01](https://www.keypedia.com/records/fda_inspections/immucor-gti-diagnostics-inc/68ec71eb-902b-4de4-9151-1274eb6d9160)

Company: https://www.keypedia.com/companies/immucor-gti-diagnostics-inc/430f7529-a30d-4723-a181-adb0037c6a21

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