FDA Inspection 1238575 — Biomat USA Inc

Biomat USA Inc — FEI 3021500737

The FDA completed an inspection of Biomat USA Inc on May 9, 2024 in Nacogdoches, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 9, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Nacogdoches, TX (United States)

Citations

IDCFRDescription
922521 CFR 606.171Biological product deviation report