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FDA Inspection
•Harold S. Boyd, MD•April 22, 2010

Harold S. Boyd, MD – FDA Inspection, Apr 22, 2010

Record Details

This FDA Inspection record concerns Harold S. Boyd, MD, with an inspection on April 22, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Harold S. Boyd, MD
Inspection Date
April 22, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 16ea3189-6174-4b84-b10f-d7c4602b6707

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
660225
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

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