FDA Inspection 1097906 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1000112586

The FDA completed an inspection of Biomat USA, Inc. on July 11, 2019 in Baton Rouge, LA. 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
July 11, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Baton Rouge, LA (United States)