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FDA Inspection
•ReNu Medical, Inc.•August 27, 2010

ReNu Medical, Inc. – FDA Inspection, Aug 27, 2010

Record Details

This FDA Inspection record concerns ReNu Medical, Inc., with an inspection on August 27, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
ReNu Medical, Inc.
Inspection Date
August 27, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · aaa3296c-e908-4e3c-835b-df32dfb71053

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
677886
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of ReNu Medical, Inc.

3
DateClassificationOfficeProject area
November 9, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
December 18, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
October 24, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for ReNu Medical, Inc.
  • FDA Inspection 1032217 - 2017-11-09
  • FDA Inspection 907486 - 2014-12-18
  • FDA Inspection 805242 - 2012-10-24

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