# FDA Inspection 1119999 - Cogentix Medical LLC - February 28, 2020

Source: https://www.keypedia.com/records/fda_inspections/cogentix-medical-llc/b4fe8874-4987-4b32-8eae-3020d4fc5d01
Source feed: FDA_Inspections

> FDA Inspection 1119999 for Cogentix Medical LLC on February 28, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1119999
- Company Name: Cogentix Medical LLC
- Inspection Date: 2020-02-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1119999 - 2020-02-28](https://www.keypedia.com/records/fda_inspections/cogentix-medical-llc/f63689a3-97ee-4663-9277-55142a86da23)
- [FDA Inspection 1024587 - 2017-08-31](https://www.keypedia.com/records/fda_inspections/cogentix-medical-llc/03772b6c-1f8e-406b-9ecb-fa5921a8b83c)
- [FDA Inspection 788335 - 2012-06-01](https://www.keypedia.com/records/fda_inspections/cogentix-medical-llc/ead46bfe-24f6-4602-97e7-b2aae3856ffc)

Company: https://www.keypedia.com/companies/cogentix-medical-llc/05b1d55c-d03c-468d-aec8-9e272a4f8b63

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