FDA Inspection 780815 — Biomat USA, Inc

Biomat USA, Inc — FEI 1038382

The FDA completed an inspection of Biomat USA, Inc on May 4, 2012 in Asheville, NC. 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
May 4, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Asheville, NC (United States)

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