FDA Inspection 594933 — Henry Ford Providence Southfield

Henry Ford Providence Southfield — FEI 1000115688

The FDA completed an inspection of Henry Ford Providence Southfield on Jun 11, 2009 in Southfield, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 11, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Southfield, MI (United States)

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