FDA Inspection 635848 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3006593072

The FDA completed an inspection of Biomat USA, Inc. on Dec 10, 2009 in Lansing, 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
Dec 10, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lansing, MI (United States)