FDA Inspection 931341 — Biomat USA Inc.

Biomat USA Inc. — FEI 3007113736

The FDA completed an inspection of Biomat USA Inc. on Jun 19, 2015 in Bristol, VA. 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
Jun 19, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bristol, VA (United States)