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FDA Inspection
•Owen Mumford USA, Inc.•March 5, 2019

FDA Inspection 1098838 - Owen Mumford USA, Inc. - March 05, 2019

Record Details

This FDA Inspection record concerns Owen Mumford USA, Inc., with an inspection on March 5, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Owen Mumford USA, Inc.
Inspection Date
March 5, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · de906999-bd20-4c4d-b78b-566273b399ab

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1098838
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Owen Mumford USA, Inc.

3
DateClassificationOfficeProject area
October 31, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
December 12, 2013OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 10, 2011VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Owen Mumford USA, Inc.
  • FDA Inspection 904740 - 2014-10-31
  • FDA Inspection 859742 - 2013-12-12
  • FDA Inspection 740437 - 2011-08-10

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