FDA Inspection 1065511 — Biomat USA, Inc

Biomat USA, Inc — FEI 3005488132

The FDA completed an inspection of Biomat USA, Inc on Aug 28, 2018 in City Of Industry, CA. 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
Aug 28, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
City Of Industry, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.