# Cogentix Medical, Inc. – FDA Inspection, May 1, 2013

Source: https://www.keypedia.com/records/fda_inspections/cogentix-medical-inc/8a35b7d1-9d06-4a5e-96a0-3041f4854baf
Source feed: FDA_Inspections

> FDA inspection 831310 of Cogentix Medical, Inc., May 01, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 831310
- Company Name: Cogentix Medical, Inc.
- Inspection Date: 2013-05-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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- [FDA Inspection 711939 - 2011-02-11](https://www.keypedia.com/records/fda_inspections/cogentix-medical-inc/5ce1c5e5-f526-4f46-9051-d13c9d4d2587)

Company: https://www.keypedia.com/companies/cogentix-medical-inc/f390823b-956f-4ec5-adcc-32c9dc279ec6

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