# Refine USA, LLC – FDA Inspection, Apr 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/refine-usa-llc/8f893699-8f3d-4230-b4cb-a24bb66f41a0
Source feed: FDA_Inspections

> FDA inspection 1049482 of Refine USA, LLC, April 18, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations 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: 1049482
- Company Name: Refine USA, LLC
- Inspection Date: 2018-04-18
- 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: 6

## Related Documents

- [FDA Inspection 1215028 - 2023-08-16](https://www.keypedia.com/records/fda_inspections/refine-usa-llc/25957ef7-6a47-46c8-b460-87533d172717)
- FDA Inspection 852060 - 2013-10-04

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

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