FDA Inspection 1150180 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005622193

The FDA completed an inspection of Biomat USA, Inc. on August 13, 2021 in San Antonio, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 13, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
San Antonio, TX (United States)