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FDA Inspection
•James N. Moy, M.D.•May 22, 2009

James N. Moy, M.D. – FDA Inspection, May 22, 2009

Record Details

This FDA Inspection record concerns James N. Moy, M.D., with an inspection on May 22, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
James N. Moy, M.D.
Inspection Date
May 22, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 7870e40d-d597-4a92-b520-c277fd1a9f67

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
583653
FDA center
Biologics
Project area
Bioresearch Monitoring

FDA Citations

1
  1. 21 CFR 312.50Ensuring compliance with plan and protocol

Full citation text and observation details available on the Dashboard.

Other FDA inspections of James N. Moy, M.D.

2
DateClassificationOfficeProject area
September 30, 2015VAICenter for Biologics Evaluation and ResearchBioresearch Monitoring
June 16, 2009VAICenter for Biologics Evaluation and ResearchBioresearch Monitoring
Other documents for James N. Moy, M.D.
  • FDA Inspection 943906 - 2015-09-30
  • FDA Inspection 589005 - 2009-06-16

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