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FDA Inspection
•Stephen G. Slade, M.D.•November 17, 2017

Stephen G. Slade, M.D. – FDA Inspection, Nov 17, 2017

Record Details

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

Company
Stephen G. Slade, M.D.
Inspection Date
November 17, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Leighton K. Ngai (Company Rep)
View Company Profile

ID · 2d1ef5cc-e834-4959-adae-5e0fc48eb0a2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1031787
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
  2. 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
  3. 21 CFR 812.140(a)(3)Investigator's subject records inadequate

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Stephen G. Slade, M.D.

2
DateClassificationOfficeProject area
May 7, 2021NAICenter for Devices and Radiological HealthBioresearch Monitoring
June 10, 2014NAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Stephen G. Slade, M.D.
  • FDA Inspection 1142734 - 2021-05-07
  • FDA Inspection 882692 - 2014-06-10

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