FDA inspection

AAK USA K1-K2 LLC: FDA inspection ending Jun 18, 2018

FDA inspection 1059778 · No Action Indicated (NAI) · Louisville, KY

Key facts

Inspection ID 1059778
Firm AAK USA K1-K2 LLC
FEI number 1037097
Address 2520 7th Street Rd
City Louisville
State KY
ZIP 40208
Country United States
Fiscal year 2018
Inspection end date Jun 18, 2018
Classification No Action Indicated (NAI)
Project area Foodborne Biological Hazards
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
  • 10–99 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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