FDA Inspection 1069823 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1038058

The FDA completed an inspection of Biomat USA, Inc. on Sep 27, 2018 in Mobile, AL. 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
Sep 27, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mobile, AL (United States)

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