FDA inspection

Lotus Brands, Inc: FDA inspection ending Dec 7, 2017

FDA inspection 1034734 · Voluntary Action Indicated (VAI) · Silver Lake, WI

Key facts

Inspection ID 1034734
Firm Lotus Brands, Inc
FEI number 1000116001
Address 1100 E Lotus Dr
City Silver Lake
State WI
ZIP 53170
Country United States
Fiscal year 2018
Inspection end date Dec 7, 2017
Classification Voluntary Action Indicated (VAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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