FDA Inspection 602373 — Virginia Center for Reproductive Medicine

Virginia Center for Reproductive Medicine — FEI 3003939253

The FDA completed an inspection of Virginia Center for Reproductive Medicine on July 29, 2009 in Reston, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 29, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Reston, VA (United States)