# FDA Inspection 1021914 - Ranir, LLC - August 16, 2017

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

> FDA Inspection 1021914 for Ranir, LLC on August 16, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1021914 - 2017-08-16](https://www.keypedia.com/records/fda_inspections/ranir-llc/1acbb713-2156-47c7-8b8c-1d6de0ad9799)
- [FDA Inspection 951697 - 2015-10-28](https://www.keypedia.com/records/fda_inspections/ranir-llc/998e76a7-e550-41db-a671-98e0cf6f9d09)
- [FDA Inspection 866413 - 2014-02-27](https://www.keypedia.com/records/fda_inspections/ranir-llc/0513378f-d39f-4043-9457-ed79d1af52c7)
- [FDA Inspection 866413 - 2014-02-27](https://www.keypedia.com/records/fda_inspections/ranir-llc/1bea4766-0aea-4a10-8a00-6fa6886e52c3)

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