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FDA Inspection
•Confluent Medical Technologies, Inc.•August 15, 2017

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

Record Details

This FDA Inspection record concerns Confluent Medical Technologies, Inc., with an inspection on August 15, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Confluent Medical Technologies, Inc.
Inspection Date
August 15, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • James A. Lane (FDA Associated Person)
View Company Profile

ID · 5a30e1e2-7728-4442-b85d-789b47f614d9

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1024251
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Confluent Medical Technologies, Inc.

4
DateClassificationOfficeProject area
April 11, 2016NAICenter 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 983442 - 2016-04-11
  • FDA Inspection 862428 - 2014-01-16
  • FDA Inspection 782811 - 2012-05-22
  • FDA Inspection 588443 - 2009-06-11

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