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FDA Inspection
•George S. Lipkowitz, M.D.•November 8, 2012

George S. Lipkowitz, M.D. – FDA Inspection, Nov 8, 2012

Record Details

This FDA Inspection record concerns George S. Lipkowitz, M.D., with an inspection on November 8, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company
George S. Lipkowitz, M.D.
Inspection Date
November 8, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 699a3baf-ba04-450e-8c9f-ad144e5c4cd3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
810110
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

FDA Citations

1
  1. 21 CFR 812.100Investigator lack of informed consent

Full citation text and observation details available on the Dashboard.

Other FDA inspections of George S. Lipkowitz, M.D.

1
DateClassificationOfficeProject area
May 10, 2018NAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for George S. Lipkowitz, M.D.
  • FDA Inspection 1053788 - 2018-05-10

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