FDA Inspection 650339 — Lotus Brands, Inc

Lotus Brands, Inc — FEI 1000116001

The FDA completed an inspection of Lotus Brands, Inc on April 8, 2010 in Silver Lake, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 8, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Silver Lake, WI (United States)

Citations

IDCFRDescription
1592221 CFR 111.95(b)(3)Documentation - ensure specifications met