FDA Inspection 947285 — Sanford Women's Health Advanced Reproductive Laboratory

Sanford Women's Health Advanced Reproductive Laboratory — FEI 3003981145

The FDA completed an inspection of Sanford Women's Health Advanced Reproductive Laboratory on September 16, 2015 in Sioux Falls, SD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 16, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Sioux Falls, SD (United States)