FDA inspection

ELOS MEDTECH PINOL A/S: FDA inspection ending Nov 21, 2013

FDA inspection 864555 · No Action Indicated (NAI) · Gorlose

Key facts

Inspection ID 864555
Firm ELOS MEDTECH PINOL A/S
FEI number 3007689689
Address Engvej 33
City Gorlose
Country Denmark
Fiscal year 2014
Inspection end date Nov 21, 2013
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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