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FDA Inspection 594933 — Henry Ford Providence Southfield

Henry Ford Providence Southfield — FEI 1000115688

The FDA completed an inspection of Henry Ford Providence Southfield on June 11, 2009 in Southfield, MI. 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 11, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Southfield, MI (United States)

Facility

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FDA data resources