FDA Inspection 935765 — Biomat USA Inc.

Biomat USA Inc. — FEI 1470275

The FDA completed an inspection of Biomat USA Inc. on Jul 20, 2015 in Chicago, 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
Jul 20, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chicago, IL (United States)