Garen Koloyan, M.D., PhD. – FDA Inspection, Jan 20, 2023

Record Details

This FDA Inspection record concerns Garen Koloyan, M.D., PhD., with an inspection on January 20, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: Garen Koloyan, M.D., PhD.
Inspection Date: January 20, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health
People: Colleen E. Burke (Company Rep)
Lori Gioia (FDA Associated Person)

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ID · 4a14658a-71bf-4a5b-9126-e8c91ef4cf6f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 1198729
FDA center: Medical Devices & Rad Health
Project area: Bioresearch Monitoring
Outcome: Form 483 issued

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FDA Inspection

Garen Koloyan, M.D., PhD.January 20, 2023