FDA Inspection 743160 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1052094

The FDA completed an inspection of Biomat USA, Inc. on Sep 8, 2011 in Jacksonville, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 8, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
922521 CFR 606.171Biological product deviation report