# FDA Inspection 889247 - Refine LLC - July 16, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/refine-llc/a982cd2a-589c-4b7a-86c1-aad08632800c
Source feed: FDA_Inspections

> FDA Inspection 889247 for Refine LLC on July 16, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 889247
- Company Name: Refine LLC
- Inspection Date: 2014-07-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [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/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