FDA Inspection 1219106 — Biomat USA Inc

Biomat USA Inc — FEI 3014948183

The FDA completed an inspection of Biomat USA Inc on Aug 24, 2023 in Fayetteville, NC. 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
Aug 24, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fayetteville, NC (United States)

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