# FDA Inspection 989123 - Rage Corporation - October 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/rage-corporation/b099632b-95b5-4fa1-bffa-367a2841838f
Source feed: FDA_Inspections

> FDA Inspection 989123 for Rage Corporation on October 20, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989123
- Company Name: Rage Corporation
- Inspection Date: 2016-10-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 989123 - 2016-10-20](https://www.keypedia.com/records/fda_inspections/rage-corporation/674ef3dc-b0d7-4c28-b3c5-59231c40053c)

Company: https://www.keypedia.com/companies/rage-corporation/02254952-8b24-4842-9ee4-e644b7cfbd4e

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