FDA Inspection 939282 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3019719

The FDA completed an inspection of Biomat USA, Inc. on August 21, 2015 in Seattle, WA. 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
August 21, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Seattle, WA (United States)