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FDA Inspection
•Mark L. Brantly, M.D.•December 11, 2009

Mark L. Brantly, M.D. – FDA Inspection, Dec 11, 2009

Record Details

This FDA Inspection record concerns Mark L. Brantly, M.D., with an inspection on December 11, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Mark L. Brantly, M.D.
Inspection Date
December 11, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 61fc5414-e3ba-4dd2-abd8-8054352acb10

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
634715
FDA center
Biologics
Project area
Bioresearch Monitoring

FDA Citations

2
  1. 21 CFR 312.60FD-1572, protocol compliance
  2. 21 CFR 312.62(b)Case history records- inadequate or inadequate

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Mark L. Brantly, M.D.

2
DateClassificationOfficeProject area
April 14, 2017NAICenter for Biologics Evaluation and ResearchBioresearch Monitoring
September 21, 2009NAICenter for Biologics Evaluation and ResearchBioresearch Monitoring
Other documents for Mark L. Brantly, M.D.
  • FDA Inspection 1012256 - 2017-04-14
  • FDA Inspection 621495 - 2009-09-21

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