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FDA Inspection
•Dr. James A. Thompson, M.D.•December 20, 2023

Dr. James A. Thompson, M.D. – FDA Inspection, Dec 20, 2023

Record Details

This FDA Inspection record concerns Dr. James A. Thompson, M.D., with an inspection on December 20, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Dr. James A. Thompson, M.D.
Inspection Date
December 20, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Emily A. Baldwin (Company Rep)
  • Valerie L Kelesyan (Issuing Officer)
View Company Profile

ID · 5805a8b7-7648-4d4a-b988-a77ab0930fe2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1225712
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

4
  1. 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
  2. 21 CFR 812.110(d)Inadequate financial disclosure by investigator
  3. 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
  4. 21 CFR 812.110(d)Inadequate financial disclosure by investigator

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Dr. James A. Thompson, M.D.

1
DateClassificationOfficeProject area
September 27, 2023VAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Dr. James A. Thompson, M.D.
  • FDA Inspection 1219465 - 2023-09-27

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