# Arrinex – FDA Inspection, Nov 9, 2018

Source: https://www.keypedia.com/records/fda_inspections/arrinex/5782e346-4fe4-4f0c-8271-59ef4a312c62
Source feed: FDA_Inspections

> FDA inspection 1075863 of Arrinex, 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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

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

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