FEI establishment

AMPLIFON

FDA establishment FEI 3002806418 · Milan, Italy

Key facts

FEI number 3002806418
Legal name AMPLIFON
City Milan
Country Italy
Product types Devices
Last inspection Jun 20, 2002

At a glance

  • 1–9 FDA inspections
  • None No Action Indicated (NAI)
  • 1–9 Voluntary Action Indicated (VAI)
  • None Official Action Indicated (OAI)
  • 1–9 Inspections with a Form 483
  • None Citations
  • None Repeat citations
  • None Warning letters
  • 1–9 Linked 510(k)s

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA establishments (FEI)

An FEI (FDA Establishment Identifier) is the number the FDA assigns to a site it inspects. FEIs of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection and compliance data

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