FDA Inspection 1078583 — Biomat USA Inc.

Biomat USA Inc. — FEI 3011714325

The FDA completed an inspection of Biomat USA Inc. on Nov 28, 2018 in Sandy, UT. 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
Nov 28, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sandy, UT (United States)

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