FDA inspection

Orkla Care AB: FDA inspection ending Sep 2, 2010

FDA inspection 683588 · Official Action Indicated (OAI) · Solna

Key facts

Inspection ID 683588
Firm Orkla Care AB
FEI number 3000182940
Address Svetsarvagen 15
City Solna
Country Sweden
Fiscal year 2010
Inspection end date Sep 2, 2010
Classification Official Action Indicated (OAI)
Project area Compliance: 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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