FDA Inspection 1119618 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3012304584

The FDA completed an inspection of Biomat USA, Inc. on January 9, 2020 in Newport News, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 9, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Newport News, VA (United States)