# FDA Inspection 983046 - GCX Corporation - May 05, 2016

Source: https://www.keypedia.com/records/fda_inspections/gcx-corporation/d2de4521-3933-42ec-a8c2-a42e00bd1491
Source feed: FDA_Inspections

> FDA Inspection 983046 for GCX Corporation on May 05, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 983046
- Company Name: GCX Corporation
- Inspection Date: 2016-05-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 983046 - 2016-05-05](https://www.keypedia.com/records/fda_inspections/gcx-corporation/937e9b0d-7e56-4974-87e7-03ca524262ad)

Company: https://www.keypedia.com/companies/gcx-corporation/b7197117-33f6-4624-86b9-9689cacf57c9

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