FDA Inspection 1232567 — Biomat USA Inc

Biomat USA Inc — FEI 3020708398

The FDA completed an inspection of Biomat USA Inc on Feb 8, 2024 in Billings, MT. 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
Feb 8, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Billings, MT (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.