FDA Inspection 847670 — Vios Fertility Institute

Vios Fertility Institute — FEI 3004114998

The FDA completed an inspection of Vios Fertility Institute on August 12, 2013 in Southfield, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 12, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Southfield, MI (United States)

Citations

IDCFRDescription
1221321 CFR 1271.47(a)Testing, screening, donor eligibility procedures
1222921 CFR 1271.50(a)Determination based on screening and testing
1227721 CFR 1271.75(a)(1)Risk factors, clinical evidence