# Confluent Medical Technologies, Inc. – FDA Inspection, Aug 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/confluent-medical-technologies-inc/5a30e1e2-7728-4442-b85d-789b47f614d9
Source feed: FDA_Inspections

> FDA inspection 1024251 of Confluent Medical Technologies, Inc., August 15, 2017. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1024251
- Company Name: Confluent Medical Technologies, Inc.
- Inspection Date: 2017-08-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 983442 - 2016-04-11](https://www.keypedia.com/records/fda_inspections/confluent-medical-technologies-inc/89a2894a-ff14-4d33-80d9-91aaf55c2737)
- FDA Inspection 862428 - 2014-01-16
- FDA Inspection 782811 - 2012-05-22
- FDA Inspection 588443 - 2009-06-11

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/james-a-lane/f6cd3d8d-7de9-45c5-9380-7e0c5de4720e)

Company: https://www.keypedia.com/companies/confluent-medical-technologies-inc/17a1ad7c-7252-40e3-a0e4-479dd07ef2b4

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