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FDA Inspection
•Confluent Medical Technologies, Inc.•April 11, 2016

Confluent Medical Technologies, Inc. – FDA Inspection, Apr 11, 2016

Record Details

This FDA Inspection record concerns Confluent Medical Technologies, Inc., with an inspection on April 11, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Confluent Medical Technologies, Inc.
Inspection Date
April 11, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 89a2894a-ff14-4d33-80d9-91aaf55c2737

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
983442
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Confluent Medical Technologies, Inc.

4
DateClassificationOfficeProject area
August 15, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
January 16, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 22, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 11, 2009NAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Confluent Medical Technologies, Inc.
  • FDA Inspection 1024251 - 2017-08-15
  • FDA Inspection 862428 - 2014-01-16
  • FDA Inspection 782811 - 2012-05-22
  • FDA Inspection 588443 - 2009-06-11

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