FDA inspection

Leoni Fiber Optics GmbH: FDA inspection ending Feb 16, 2017

FDA inspection 1004235 · No Action Indicated (NAI) · Foritztal

Key facts

Inspection ID 1004235
Firm Leoni Fiber Optics GmbH
FEI number 3005128587
Address Muhldamm 6
City Foritztal
Country Germany
Fiscal year 2017
Inspection end date Feb 16, 2017
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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