FDA Inspection 1028343 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3002793370

The FDA completed an inspection of Biomat USA, Inc. on September 20, 2017 in Wichita Falls, TX. 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
September 20, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wichita Falls, TX (United States)