FDA Inspection 1025643 — Biomat USA Inc

Biomat USA Inc — FEI 3012230191

The FDA completed an inspection of Biomat USA Inc on September 7, 2017 in Greenville, NC. 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
September 7, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Greenville, NC (United States)