# FDA Inspection 1109222 - GURIN PRODUCTS LLC - November 08, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/gurin-products-llc/bfd0d3e2-ad70-45ff-8d00-fe7ac8d5ba16
Source feed: FDA_Inspections

> FDA Inspection 1109222 for GURIN PRODUCTS LLC on November 08, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1109222
- Company Name: GURIN PRODUCTS LLC
- Inspection Date: 2019-11-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1109222 - 2019-11-08](https://www.globalkeysolutions.net/records/fda_inspections/gurin-products-llc/40e8ae4c-af2a-4ca4-9ed9-f52eae80efb3)

Company: https://www.globalkeysolutions.net/companies/gurin-products-llc/2e16063c-70d7-491b-9aa7-0ae7fe16a761

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