FDA Inspection 1237463 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3012263919

The FDA completed an inspection of Biomat USA, Inc. on Apr 26, 2024 in Merrillville, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 26, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Merrillville, IN (United States)