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FDA Inspection 1056801 — Kofinas Fertility Group

Kofinas Fertility Group — FEI 3004753467

The FDA completed an inspection of Kofinas Fertility Group on June 25, 2018 in New York, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 25, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
New York, NY (United States)

Facility

Other inspections at this facility

  • 1266536 (VAI Wed Apr 09 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1210757 (VAI Tue Jul 25 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1122513 (NAI Thu Feb 13 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 963390 (NAI Fri Mar 11 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 857553 (NAI Wed Dec 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources