FDA Inspection 1327274 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3013951395

The FDA completed an inspection of Biomat USA, Inc. on Jul 15, 2026 in Lancaster, CA. 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
Jul 15, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lancaster, CA (United States)

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