# FDA Inspection 732926 - UreSil LLC - June 30, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/uresil-llc/dfdb369d-4ce7-47cf-b1d7-db7d94da440d
Source feed: FDA_Inspections

> FDA Inspection 732926 for UreSil LLC on June 30, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 732926
- Company Name: UreSil LLC
- Inspection Date: 2011-06-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 914523 - 2015-01-27](https://www.globalkeysolutions.net/records/fda_inspections/uresil-llc/d01ea109-483a-4e27-97ed-bba9fd1e6ed6)
- [FDA Inspection 732926 - 2011-06-30](https://www.globalkeysolutions.net/records/fda_inspections/uresil-llc/55678fd6-c323-473b-b3d3-69e29d5d0a22)

Company: https://www.globalkeysolutions.net/companies/uresil-llc/783ed6c8-45aa-496c-98d3-542c4af3c91e

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