FDA inspection

LEK Pharmaceuticals d.d.: FDA inspection ending Jul 2, 2002

FDA inspection 232299 · No Action Indicated (NAI) · Menges

Key facts

Inspection ID 232299
Firm LEK Pharmaceuticals d.d.
FEI number 3002807470
Address Kolodvorska cesta 27
City Menges
Fiscal year 2002
Inspection end date Jul 2, 2002
Classification No Action Indicated (NAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

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