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FDA Inspection 1024608 — Sanford Reproductive Medicine

Sanford Reproductive Medicine — FEI 3005043101

The FDA completed an inspection of Sanford Reproductive Medicine on August 14, 2017 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
August 14, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fargo, ND (United States)

Facility

Other inspections at this facility

  • 1271181 (NAI Wed Apr 30 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1172544 (NAI Tue May 31 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 896591 (NAI Tue Sep 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 759809 (NAI Wed Dec 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 674329 (NAI Mon Aug 02 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources