FDA Inspection 1044110 — Biomat USA Inc

Biomat USA Inc — FEI 3011626200

The FDA completed an inspection of Biomat USA Inc on Mar 2, 2018 in Austin, 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). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 2, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Austin, TX (United States)

Citations

IDCFRDescription
15921 CFR 606.160(a)(1)Legibility and indelibility
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs