FDA Inspection 1044390 — Biomat USA Inc

Biomat USA Inc — FEI 3007011613

The FDA completed an inspection of Biomat USA Inc on Feb 13, 2018 in New Orleans, LA. 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
Feb 13, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
New Orleans, LA (United States)