FDA Inspection 1101901 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3007172302

The FDA completed an inspection of Biomat USA, Inc. on August 20, 2019 in Yuma, AZ. 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 20, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Yuma, AZ (United States)