# FDA Inspection 901650 - Enuresis Solutions, LLC - October 30, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/enuresis-solutions-llc/df1b2ad4-abe1-431e-9cdd-2f20d168237a
Source feed: FDA_Inspections

> FDA Inspection 901650 for Enuresis Solutions, LLC on October 30, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 901650
- Company Name: Enuresis Solutions, LLC
- Inspection Date: 2014-10-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1083916 - 2019-03-26](https://www.globalkeysolutions.net/records/fda_inspections/enuresis-solutions-llc/727149fe-32f5-48fa-97f9-16eca3c8df69)
- [FDA Inspection 901650 - 2014-10-30](https://www.globalkeysolutions.net/records/fda_inspections/enuresis-solutions-llc/0999c5e3-7faa-4b47-b8f1-864da3f5bb77)

Company: https://www.globalkeysolutions.net/companies/enuresis-solutions-llc/4a543cfd-f8ed-43b3-ac67-8aabd92b9437

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