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FDA Inspection
•Thomas E. Van Dyke, DDS, PhD•March 31, 2016

Thomas E. Van Dyke, DDS, PhD – FDA Inspection, Mar 31, 2016

Record Details

This FDA Inspection record concerns Thomas E. Van Dyke, DDS, PhD, with an inspection on March 31, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Thomas E. Van Dyke, DDS, PhD
Inspection Date
March 31, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c38acf3c-1139-4091-947d-e8e2bb6afdb1

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
968162
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

FDA Citations

2
  1. 21 CFR 812.7(d)Investigational device represented as safe and /or effective
  2. 21 CFR 812.110(d)Inadequate financial disclosure by investigator

Full citation text and observation details available on the Dashboard.

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