FDA Inspection 703347 — Biomat USA Inc

Biomat USA Inc — FEI 3000215056

The FDA completed an inspection of Biomat USA Inc on Dec 28, 2010 in Clearwater, FL. 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
Dec 28, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Clearwater, FL (United States)

Citations

IDCFRDescription
33821 CFR 640.65(b)(2)(i)Physician review of four month sample
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs