FDA inspection

Vistin Pharma AS avd Kragero Fikkjebakke: FDA inspection ending Jul 4, 2014

FDA inspection 892560 · Voluntary Action Indicated (VAI) · Sannidal

Key facts

Inspection ID 892560
Firm Vistin Pharma AS avd Kragero Fikkjebakke
FEI number 3006272184
Address Stuttlidalen 4
City Sannidal
Country Norway
Fiscal year 2014
Inspection end date Jul 4, 2014
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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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