FDA Inspection 808143 — Biomat Usa Inc

Biomat Usa Inc — FEI 3001236857

The FDA completed an inspection of Biomat Usa Inc on November 16, 2012 in San Diego, CA. 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 16, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Diego, CA (United States)