FDA Inspection 885532 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3003832406

The FDA completed an inspection of Biomat USA, Inc. on June 18, 2014 in Hampton, 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
June 18, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Hampton, VA (United States)