# FDA Inspection 977541 - Immucor GTI Diagnostics, Inc - February 01, 2016

Source: https://www.keypedia.com/records/fda_inspections/immucor-gti-diagnostics-inc/68ec71eb-902b-4de4-9151-1274eb6d9160
Source feed: FDA_Inspections

> FDA Inspection 977541 for Immucor GTI Diagnostics, Inc on February 01, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 977541
- Company Name: Immucor GTI Diagnostics, Inc
- Inspection Date: 2016-02-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: 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 639478 - 2010-01-13](https://www.keypedia.com/records/fda_inspections/immucor-gti-diagnostics-inc/97a94f54-cdcc-4320-959c-b8645a3f5b01)

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