# UreSil LLC – FDA Inspection, Jan 27, 2015

Source: https://www.keypedia.com/records/fda_inspections/uresil-llc/d01ea109-483a-4e27-97ed-bba9fd1e6ed6
Source feed: FDA_Inspections

> FDA inspection 914523 of UreSil LLC, January 27, 2015. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 914523
- Company Name: UreSil LLC
- Inspection Date: 2015-01-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 732926 - 2011-06-30

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

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