FDA inspection

FMS, Finapres Medical Systems BV: FDA inspection ending May 20, 2008

FDA inspection 521653 · No Action Indicated (NAI) · Amsterdam Zuidoost

Key facts

Inspection ID 521653
Firm FMS, Finapres Medical Systems BV
FEI number 3003803088
Address Paasheuvelweg 34A, 1105 BJ
City Amsterdam Zuidoost
Fiscal year 2008
Inspection end date May 20, 2008
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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