# FDA Inspection 900085 - RMD, LLC - October 17, 2014

Source: https://www.keypedia.com/records/fda_inspections/rmd-llc/87fb4c40-4990-488b-a051-bb88e95c71e3
Source feed: FDA_Inspections

> FDA Inspection 900085 for RMD, LLC on October 17, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900085
- Company Name: RMD, LLC
- Inspection Date: 2014-10-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 900085 - 2014-10-17](https://www.keypedia.com/records/fda_inspections/rmd-llc/823a3689-4f39-43ff-8fc3-f6e031058b20)

Company: https://www.keypedia.com/companies/rmd-llc/21a7dc9d-8dea-4da9-a8c7-09fdef7f5bd5

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