FDA inspection

Abigo Medical AB: FDA inspection ending Jan 30, 2018

FDA inspection 1043750 · No Action Indicated (NAI) · Molndal

Key facts

Inspection ID 1043750
Firm Abigo Medical AB
FEI number 3004017406
Address Ekonomivagen 5
City Molndal
Country Sweden
Fiscal year 2018
Inspection end date Jan 30, 2018
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

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