FDA inspection

Arjo Med. AB: FDA inspection ending Oct 8, 1999

FDA inspection 3455 · No Action Indicated (NAI) · Gloucester

Key facts

Inspection ID 3455
Firm Arjo Med. AB
FEI number 3002806396
Address St. Catherine Street
City Gloucester
Fiscal year 2000
Inspection end date Oct 8, 1999
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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