FDA inspection

Baxter Althin Medical AB: FDA inspection ending Jan 17, 2002

FDA inspection 204433 · No Action Indicated (NAI) · Ronneby

Key facts

Inspection ID 204433
Firm Baxter Althin Medical AB
FEI number 3001267558
Address Box 39, Fridhemsvagen 15
City Ronneby
Fiscal year 2002
Inspection end date Jan 17, 2002
Classification No Action Indicated (NAI)
Project area Compliance: Med 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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