FDA Inspection 1254807 — Biomat USA

Biomat USA — FEI 3013758223

The FDA completed an inspection of Biomat USA on November 7, 2024 in Meridian, MS. 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
November 7, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Meridian, MS (United States)