# FDA Inspection 1049482 - Refine USA, LLC - April 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/refine-usa-llc/160fbfc8-1f6d-4c9a-ba50-e958a1d6bcbf
Source feed: FDA_Inspections

> FDA Inspection 1049482 for Refine USA, LLC on April 18, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1049482
- Company Name: Refine USA, LLC
- Inspection Date: 2018-04-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/refine-usa-llc/52f6174e-99ed-4128-9380-d6434537b084

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