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FDA Inspection 1013350 — Henry Ford Providence Southfield

Henry Ford Providence Southfield — FEI 1000115688

The FDA completed an inspection of Henry Ford Providence Southfield on May 8, 2017 in Southfield, MI. 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
May 8, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Southfield, MI (United States)

Facility

Other inspections at this facility

  • 1252649 (NAI Thu Oct 10 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1105841 (NAI Tue Sep 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 926598 (NAI Thu May 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 836796 (NAI Thu Jun 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817370 (NAI Wed Jan 23 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources