FDA Inspection 701682 — Midwest Fertility Center

Midwest Fertility Center — FEI 3003966448

The FDA completed an inspection of Midwest Fertility Center on December 14, 2010 in Downers Grove, IL. 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
December 14, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Downers Grove, IL (United States)