FDA inspection

Danipharm A/S: FDA inspection ending Mar 4, 2015

FDA inspection 917909 · Voluntary Action Indicated (VAI) · Nibe

Key facts

Inspection ID 917909
Firm Danipharm A/S
FEI number 3002806781
Address Skalhuse 3
City Nibe
Country Denmark
Fiscal year 2015
Inspection end date Mar 4, 2015
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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