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FDA Inspection
•Roberto Vieira Botelho, MD•May 8, 2015

Roberto Vieira Botelho, MD – FDA Inspection, May 8, 2015

Record Details

This FDA Inspection record concerns Roberto Vieira Botelho, MD, with an inspection on May 8, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Roberto Vieira Botelho, MD
Inspection Date
May 8, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 7938ffaa-6b61-497b-ad4f-7659d4fa71bf

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
927964
FDA center
Human Drugs
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 Roberto Vieira Botelho, MD

1
DateClassificationOfficeProject area
November 19, 2011NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Roberto Vieira Botelho, MD
  • FDA Inspection 756430 - 2011-11-19

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