FDA Inspection 1181929 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3013002402

The FDA completed an inspection of Biomat USA, Inc. on Oct 14, 2022 in Carrollton, TX. 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
Oct 14, 2022
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Carrollton, TX (United States)

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