# FDA Inspection 988544 - Refine LLC - September 09, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/refine-llc/d9e03867-8bc9-45f2-89ff-207237a24ddd
Source feed: FDA_Inspections

> FDA Inspection 988544 for Refine LLC on September 09, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988544
- Company Name: Refine LLC
- Inspection Date: 2016-09-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 988544 - 2016-09-09](https://www.globalkeysolutions.net/records/fda_inspections/refine-llc/92803438-6cfa-4464-81f4-5e93d378fb4a)
- [FDA Inspection 889247 - 2014-07-16](https://www.globalkeysolutions.net/records/fda_inspections/refine-llc/a982cd2a-589c-4b7a-86c1-aad08632800c)
- [FDA Inspection 889247 - 2014-07-16](https://www.globalkeysolutions.net/records/fda_inspections/refine-llc/e8c8a58f-b37c-452a-98c8-04266d8723d4)

Company: https://www.globalkeysolutions.net/companies/refine-llc/55512bc2-57e9-4631-baff-bd2e05f145c8

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