Home / Inspections / 771978

FDA Inspection 771978 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1831100

The FDA completed an inspection of Biomat USA, Inc. on March 9, 2012 in South Bend, IN. 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
March 9, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
South Bend, IN (United States)

Facility

Other inspections at this facility

  • 1108083 (NAI Mon Oct 21 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1028805 (NAI Fri Sep 29 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 572502 (VAI Fri Mar 27 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources