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FDA Inspection 1116504 — Biomat USA Inc

Biomat USA Inc — FEI 3004040118

The FDA completed an inspection of Biomat USA Inc on January 15, 2020 in Council Bluffs, IA. 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
January 15, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Council Bluffs, IA (United States)

Facility

Other inspections at this facility

  • 1009236 (NAI Fri Apr 07 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 923750 (NAI Mon Apr 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 833195 (NAI Wed May 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 718878 (NAI Fri Apr 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources