FDA Inspection 1067658 — Bimoat Usa Inc

Bimoat Usa Inc — FEI 3000206206

The FDA completed an inspection of Bimoat Usa Inc on Aug 29, 2018 in Rockford, IL. 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 29, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rockford, IL (United States)