FDA inspection

Ambu A/S: FDA inspection ending Jun 19, 2013

FDA inspection 841588 · No Action Indicated (NAI) · Ballerup

Key facts

Inspection ID 841588
Firm Ambu A/S
FEI number 3002806359
Address Baltorpbakken 13
City Ballerup
Country Denmark
Fiscal year 2013
Inspection end date Jun 19, 2013
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

Browse all FDA inspections