FDA inspection

Nostrum Laboratories Inc: FDA inspection ending Apr 15, 2011

FDA inspection 720202 · Voluntary Action Indicated (VAI) · Kansas City, MO

Key facts

Inspection ID 720202
Firm Nostrum Laboratories Inc
FEI number 1930436
Address 1800 N Topping Ave
City Kansas City
State MO
ZIP 64120-1228
Fiscal year 2011
Inspection end date Apr 15, 2011
Classification Voluntary Action Indicated (VAI)
Project area Generic Drug Evaluation
Product type Drugs

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
  • 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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