FDA inspection

Sonesta Medical AB: FDA inspection ending Jun 14, 2017

FDA inspection 1014756 · Voluntary Action Indicated (VAI) · Solna

Key facts

Inspection ID 1014756
Firm Sonesta Medical AB
FEI number 3010496070
Address Tegeluddsvagen 76
City Solna
Country Sweden
Fiscal year 2017
Inspection end date Jun 14, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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

Browse all FDA inspections