FDA inspection

ALS Scandinavia AB: FDA inspection ending May 16, 2014

FDA inspection 884648 · Voluntary Action Indicated (VAI) · Lulea

Key facts

Inspection ID 884648
Firm ALS Scandinavia AB
FEI number 3007165135
Address Aurorum 10
City Lulea
Country Sweden
Fiscal year 2014
Inspection end date May 16, 2014
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
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
  • 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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