FDA Inspection 1059921 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 2077732

The FDA completed an inspection of Biomat USA, Inc. on Jul 25, 2018 in Van Nuys, CA. 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
Jul 25, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Van Nuys, CA (United States)

Citations

IDCFRDescription
922521 CFR 606.171Biological product deviation report