FDA Inspection 1066578 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1673491

The FDA completed an inspection of Biomat USA, Inc. on Aug 17, 2018 in San Antonio, TX. 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 17, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Antonio, TX (United States)