FDA Inspection 1096859 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3013440816

The FDA completed an inspection of Biomat USA, Inc. on Jun 27, 2019 in Nashville, TN. 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
Jun 27, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Nashville, TN (United States)

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