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FDA Inspection
•Orthomerica Products, Inc.•August 26, 2016

Orthomerica Products, Inc. – FDA Inspection, Aug 26, 2016

Record Details

This FDA Inspection record concerns Orthomerica Products, Inc., with an inspection on August 26, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Orthomerica Products, Inc.
Inspection Date
August 26, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · f61317e3-6255-4a80-85ed-dea8d0b3796f

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
985992
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Orthomerica Products, Inc.

2
DateClassificationOfficeProject area
May 7, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
September 10, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Orthomerica Products, Inc.
  • FDA Inspection 830911 - 2013-05-07
  • FDA Inspection 611156 - 2009-09-10

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