FDA Inspection 759809 — Sanford Reproductive Medicine

Sanford Reproductive Medicine — FEI 3005043101

The FDA completed an inspection of Sanford Reproductive Medicine on December 21, 2011 in Fargo, ND. 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
December 21, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Fargo, ND (United States)