# FDA Inspection 852060 - Refine USA, LLC - October 04, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/refine-usa-llc/fb42ac19-1208-4965-8376-49a7a2d9a726/
Source feed: FDA_Inspections

> FDA Inspection 852060 for Refine USA, LLC on October 04, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 852060
- Company Name: Refine USA, LLC
- Inspection Date: 2013-10-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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