# Urocare Products, Inc. – FDA Inspection, Dec 7, 2018

Source: https://www.keypedia.com/records/fda_inspections/urocare-products-inc/65621573-95e8-427d-a044-58e87dac112c
Source feed: FDA_Inspections

> FDA inspection 1079696 of Urocare Products, Inc., December 07, 2018. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079696
- Company Name: Urocare Products, Inc.
- Inspection Date: 2018-12-07
- 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 1233269 - 2024-02-05](https://www.keypedia.com/records/fda_inspections/urocare-products-inc/38f76d61-d7ef-4dac-b959-43c0f11a2fb6)
- FDA Inspection 791642 - 2012-07-18

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sonya-l-karsik/c24603b9-5ca0-46f5-861a-b367155b0def)

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

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