FDA Inspection 1201080 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3000718117

The FDA completed an inspection of Biomat USA, Inc. on March 24, 2023 in Anderson, IN. 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
March 24, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Anderson, IN (United States)