# FDA Inspection 791642 - Urocare Products, Inc. - July 18, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/urocare-products-inc/2f8be295-cb8d-440d-93c7-649f0b1ba1eb
Source feed: FDA_Inspections

> FDA Inspection 791642 for Urocare Products, Inc. on July 18, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791642
- Company Name: Urocare Products, Inc.
- Inspection Date: 2012-07-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1079696 - 2018-12-07](https://www.globalkeysolutions.net/records/fda_inspections/urocare-products-inc/4d8644b9-c9ad-4680-b5e6-cd39cbf6e210)
- [FDA Inspection 1079696 - 2018-12-07](https://www.globalkeysolutions.net/records/fda_inspections/urocare-products-inc/65621573-95e8-427d-a044-58e87dac112c)

Company: https://www.globalkeysolutions.net/companies/urocare-products-inc/1bcab3bd-22f7-434d-adb9-7c3d138a39e1

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