# FDA Inspection 1075863 - Arrinex - November 09, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/arrinex/0fc17689-5a29-4efd-82ab-3d688d4ccef3
Source feed: FDA_Inspections

> FDA Inspection 1075863 for Arrinex on November 09, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1075863
- Company Name: Arrinex
- Inspection Date: 2018-11-09
- 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 1075863 - 2018-11-09](https://www.globalkeysolutions.net/records/fda_inspections/arrinex/5782e346-4fe4-4f0c-8271-59ef4a312c62)

Company: https://www.globalkeysolutions.net/companies/arrinex/ed0b5236-dc74-4e02-a2c1-5bbc2dc0b5a6

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