# Ranir, LLC – FDA Inspection, Aug 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/ranir-llc/47ff44a1-a591-4ed1-bd08-cd460c4e4dfe
Source feed: FDA_Inspections

> FDA inspection 1021914 of Ranir, LLC, August 16, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021914
- Company Name: Ranir, LLC
- Inspection Date: 2017-08-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 951697 - 2015-10-28
- [FDA Inspection 866413 - 2014-02-27](https://www.keypedia.com/records/fda_inspections/ranir-llc/1bea4766-0aea-4a10-8a00-6fa6886e52c3)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/ranir-llc/846b8275-aff3-4d31-932a-302680522c27

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