Grethe Andersen, M.D. – FDA Inspection, Nov 17, 2017

Record Details

This FDA Inspection record concerns Grethe Andersen, M.D., with an inspection on November 17, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Grethe Andersen, M.D.
Inspection Date: November 17, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Corrine M. Carter (Company Rep)

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ID · cb081eb7-d0c8-43eb-98a6-c81d54da3b0e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number: 1035710
FDA center: Medical Devices & Rad Health
Project area: Bioresearch Monitoring

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FDA Inspection

Grethe Andersen, M.D.November 17, 2017