FDA inspection

Lee Products Company: FDA inspection ending Aug 9, 2005

FDA inspection 389649 · No Action Indicated (NAI) · Minneapolis, MN

Key facts

Inspection ID 389649
Firm Lee Products Company
FEI number 2111564
Address 800 E 80th St
City Minneapolis
State MN
ZIP 55420-1321
Fiscal year 2005
Inspection end date Aug 9, 2005
Classification No Action Indicated (NAI)
Project area Colors and Cosmetics Technology
Product type Food/Cosmetics

At a glance

  • None Citations
  • None 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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