FDA Inspection 702178 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3006521911

The FDA completed an inspection of Biomat USA, Inc. on Dec 16, 2010 in Mcallen, 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
Dec 16, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mcallen, TX (United States)