FDA Inspection 732609 — Biomat USA Inc

Biomat USA Inc — FEI 3006306298

The FDA completed an inspection of Biomat USA Inc on Jun 23, 2011 in Shreveport, 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
Jun 23, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Shreveport, LA (United States)