FDA Inspection 837799 — Midwest Fertility Center

Midwest Fertility Center — FEI 3003966448

The FDA completed an inspection of Midwest Fertility Center on July 2, 2013 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 2, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Downers Grove, IL (United States)

Citations

IDCFRDescription
1223621 CFR 1271.55(a)(2)Eligibility statement--basis of determination