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FDA Inspection
•John F. Ward III, MD•December 1, 2011

John F. Ward III, MD – FDA Inspection, Dec 1, 2011

Record Details

This FDA Inspection record concerns John F. Ward III, MD, with an inspection on December 1, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
John F. Ward III, MD
Inspection Date
December 1, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 0711af25-9cf6-4b77-b9c0-33cce0911f5f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
756272
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

FDA Citations

3
  1. 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
  2. 21 CFR 812.100Investigator lack of informed consent
  3. 21 CFR 812.140(a)(2)(i)Investigator device accountability inadequate

Full citation text and observation details available on the Dashboard.

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