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FDA Inspection 806108 — Biomat USA, Inc

Biomat USA, Inc — FEI 2377779

The FDA completed an inspection of Biomat USA, Inc on November 1, 2012 in Bellflower, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 1, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bellflower, CA (United States)

Facility

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FDA data resources