FDA Inspection 615009 — Biomat USA Inc

Biomat USA Inc — FEI 3005568732

The FDA completed an inspection of Biomat USA Inc on Sep 25, 2009 in Inkster, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 25, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Inkster, MI (United States)