FDA Inspection 570532 — Ultralite Enterprises Inc

Ultralite Enterprises Inc — FEI 1045025

The FDA completed an inspection of Ultralite Enterprises Inc on Jan 29, 2009 in Dacula, GA. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 29, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Dacula, GA (United States)

Citations

IDCFRDescription
368821 CFR 820.100(a)(1)Analysis of data/reports from data sources