FDA inspection

Ambu A/S: FDA inspection ending Mar 10, 2005

FDA inspection 375270 · Voluntary Action Indicated (VAI) · Ballerup

Key facts

Inspection ID 375270
Firm Ambu A/S
FEI number 3002806359
Address Baltorpbakken 13
City Ballerup
Fiscal year 2005
Inspection end date Mar 10, 2005
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

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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