FDA inspection

Fredriksons Verkstad AB: FDA inspection ending Oct 12, 2012

FDA inspection 803780 · Voluntary Action Indicated (VAI) · Vadstena

Key facts

Inspection ID 803780
Firm Fredriksons Verkstad AB
FEI number 3009709474
Address Kronangsgatan 4
City Vadstena
Country Sweden
Fiscal year 2013
Inspection end date Oct 12, 2012
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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

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