FDA Inspection 1271181 — Sanford Reproductive Medicine

Sanford Reproductive Medicine — FEI 3005043101

The FDA completed an inspection of Sanford Reproductive Medicine on Apr 30, 2025 in Fargo, ND. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 30, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Fargo, ND (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.