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FDA Inspection
•Uromedica Inc.•January 11, 2017

Uromedica Inc. – FDA Inspection, Jan 11, 2017

Record Details

This FDA Inspection record concerns Uromedica Inc., with an inspection on January 11, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Uromedica Inc.
Inspection Date
January 11, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Benjamin W. Anderson (Issuing Officer)
View Company Profile

ID · ab195fa4-9cfa-4064-ba94-7d71a29a164b

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
997754
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Uromedica Inc.

3
DateClassificationOfficeProject area
December 6, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
November 7, 2013NAICenter for Devices and Radiological HealthBioresearch Monitoring
December 19, 2008NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Uromedica Inc.
  • FDA Inspection 858993 - 2013-12-06
  • FDA Inspection 854655 - 2013-11-07
  • FDA Inspection 551123 - 2008-12-19

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