FDA inspection

Lotus Brands, Inc: FDA inspection ending Mar 11, 2015

FDA inspection 921669 · No Action Indicated (NAI) · Silver Lake, WI

Key facts

Inspection ID 921669
Firm Lotus Brands, Inc
FEI number 1000116001
Address 1100 E Lotus Dr
City Silver Lake
State WI
ZIP 53170
Country United States
Fiscal year 2015
Inspection end date Mar 11, 2015
Classification No Action Indicated (NAI)
Project area Food Composition, Standards, Labeling and Econ
Product type Food/Cosmetics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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