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FDA Inspection
•Schiffmann, Raphael MD•January 23, 2012

Schiffmann, Raphael MD – FDA Inspection, Jan 23, 2012

Record Details

This FDA Inspection record concerns Schiffmann, Raphael MD, with an inspection on January 23, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Schiffmann, Raphael MD
Inspection Date
January 23, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 9d201d4b-7f79-4e97-862e-dd7cf0192d5d

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
764126
FDA center
Human Drugs
Project area
Bioresearch Monitoring

FDA Citations

3
  1. 21 CFR 312.60FD-1572, protocol compliance
  2. 21 CFR 312.60Informed consent
  3. 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 Schiffmann, Raphael MD

1
DateClassificationOfficeProject area
September 24, 2020NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Schiffmann, Raphael MD
  • FDA Inspection 1131376 - 2020-09-24

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