FDA Inspection 1040706 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3003103935

The FDA completed an inspection of Biomat USA, Inc. on Jan 11, 2018 in Danville, 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
Jan 11, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Danville, VA (United States)

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