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FDA Inspection
•Anne Greist, MD•March 12, 2014

Anne Greist, MD – FDA Inspection, Mar 12, 2014

Record Details

This FDA Inspection record concerns Anne Greist, MD, with an inspection on March 12, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Anne Greist, MD
Inspection Date
March 12, 2014
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · bc3904be-bcb2-4cf1-9b6f-dd10cb420805

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
869532
FDA center
Biologics
Project area
Bioresearch Monitoring

FDA Citations

5
  1. 21 CFR 312.60FD-1572, protocol compliance
  2. 21 CFR 312.66Initial and continuing review
  3. 21 CFR 312.62(b)Case history records- inadequate or inadequate
  4. 21 CFR 312.66Unanticipated problems
  5. 21 CFR 312.66Changes in research

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