FDA Inspection 1209304 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3006576463

The FDA completed an inspection of Biomat USA, Inc. on June 15, 2023 in Little Rock, AR. 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 15, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Little Rock, AR (United States)